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Sample records for wastewater organic compounds

  1. ORGANIC COMPOUNDS IN ORGANOPHOSPHORUS PESTICIDE MANUFACTURING WASTEWATERS

    EPA Science Inventory

    Preliminary survey information on the organophosphorus pesticide industry wastewater streams and analytical methods to monitor levels of organic compounds present in these streams are presented. The identification and quantification of organophosphorus compounds was emphasized, b...

  2. Non-targeted analyses of organic compounds in urban wastewater.

    PubMed

    Alves Filho, Elenilson G; Sartori, Luci; Silva, Lorena M A; Silva, Bianca F; Fadini, Pedro S; Soong, Ronald; Simpson, Andre; Ferreira, Antonio G

    2015-09-01

    A large number of organic pollutants that cause damage to the ecosystem and threaten human health are transported to wastewater treatment plants (WWTPs). The problems regarding water pollution in Latin America have been well documented, and there is no evidence of substantive efforts to change the situation. In the present work, two methods to study wastewater samples are employed: non-targeted 1D ((13)C and (1)H) and 2D NMR spectroscopic analysis to characterize the largest possible number of compounds from urban wastewater and analysis by HPLC-(UV/MS)-SPE-ASS-NMR to detect non-specific recalcitrant organic compounds in treated wastewater without the use of common standards. The set of data is composed of several compounds with the concentration ranging considerably with treatment and seasonality. An anomalous discharge, the influence of stormwater on the wastewater composition and the presence of recalcitrant compounds (linear alkylbenzene sulfonate surfactant homologs) in the effluent were further identified. The seasonal variations and abnormality in the composition of organic compounds in sewage indicated that the procedure that was employed can be useful in the identification of the pollution source and to enhance the effectiveness of WWTPs in designing preventive action to protect the equipment and preserve the environment. PMID:25354334

  3. IDENTIFICATION OF ORGANIC COMPOUNDS IN AN INDUSTRIAL WASTEWATER

    EPA Science Inventory

    Gas chromatography/mass spectrometry (GC/MS) was used in a survey analysis of organic compounds in an industrial wastewater. Problems in the interpretation of the GC/MS data in effluent from a specialty chemicals plant were addressed. An important feature of the study was the use...

  4. Fate of Volatile Organic Compounds in Constructed Wastewater Treatment Wetlands

    USGS Publications Warehouse

    Keefe, S.H.; Barber, L.B.; Runkel, R.L.; Ryan, J.N.

    2004-01-01

    The fate of volatile organic compounds was evaluated in a wastewater-dependent constructed wetland near Phoenix, AZ, using field measurements and solute transport modeling. Numerically based volatilization rates were determined using inverse modeling techniques and hydraulic parameters established by sodium bromide tracer experiments. Theoretical volatilization rates were calculated from the two-film method incorporating physicochemical properties and environmental conditions. Additional analyses were conducted using graphically determined volatilization rates based on field measurements. Transport (with first-order removal) simulations were performed using a range of volatilization rates and were evaluated with respect to field concentrations. The inverse and two-film reactive transport simulations demonstrated excellent agreement with measured concentrations for 1,4-dichlorobenzene, tetrachloroethene, dichloromethane, and trichloromethane and fair agreement for dibromochloromethane, bromo-dichloromethane, and toluene. Wetland removal efficiencies from inlet to outlet ranged from 63% to 87% for target compounds.

  5. MULTISPECTRAL IDENTIFICATION AND CONFIRMATION OF ORGANIC COMPOUNDS IN WASTEWATER EXTRACTS

    EPA Science Inventory

    Application of multispectral identification techniques to samples from industrial and POTW wastewaters revealed identities of 63 compounds that had not been identified by empirical matching of mass spectra with spectral libraries. wenty-five of the compounds had not been found in...

  6. Stripping of organic compounds from wastewater as an auxiliary fuel of regenerative thermal oxidizer.

    PubMed

    Chang, Meng-Wen; Chern, Jia-Ming

    2009-08-15

    Organic solvents with different volatilities are widely used in various processes and generate air and water pollution problems. In the cleaning processes of electronics industries, most volatile organic compounds (VOCs) are vented to air pollution control devices while most non-volatile organic solvents dissolve in the cleaning water and become the major sources of COD in wastewater. Discharging a high-COD wastewater stream to wastewater treatment facility often disturbs the treatment performance. A pretreatment of the high-COD wastewater is therefore highly desirable. This study used a packed-bed stripping tower in combination with a regenerative thermal oxidizer to remove the COD in the wastewater from a printed circuit board manufacturing process and to utilize the stripped organic compounds as the auxiliary fuel of the RTO. The experimental results showed that up to 45% of the COD could be removed and 66% of the RTO fuel could be saved by the combined treatment system. PMID:19195779

  7. PARTITIONING OF TOXIC ORGANIC COMPOUNDS ON MUNICIPAL WASTEWATER TREATMENT PLANT SOLIDS

    EPA Science Inventory

    Fundamental aspects of partitioning of toxic organic compounds on municipal wastewater treatment plant solids have been investigated. Sorption on wastewater solids was not affected by solids-to-liquid ratio. Kinetic data on sorption showed an initial rapid uptake followed by a sl...

  8. Removal of dioxins, PCB's and other halogenated organic compounds from wastewater

    SciTech Connect

    Ying, W.C.; Sojka, S.A.

    1986-11-18

    This patent describes the combination of physicochemical and biological treatment processes for removing dioxins, PCB's, and other halogenated organic compounds from raw wastewater, in a pretreatment zone to produce pretreated wastewater still containing minor proportions, of dioxins and PCB's and then in a reaction zone wherein final effluent is produced. This comprises the physiocochemical process consisting of subjecting the raw wastewater to simultaneous neutralization and oxidation, followed by separating precipitated products, which precipitated products have adsorbed a major proportion of at least 90% of the dioxins and PCB's present in the raw wastewater in the same pretreatment zone. It is then followed by biological treatment process consisting of subjecting the pre-treated wastewater, which contains the minor proportion of dioxins and PCB's, and other halogenated organic compounds in raw wastewater, to a combined powdered active carbon adsorption and biological treatment process in a sequencing batch reactor in the presence of acclimated activated sludge. This process comprises the steps FILL, REACT, SETTLE, DRAW, and IDLE. The combined treatment process operates at a mixed liquor suspended solids concentration in excess of 5000 mg/L, and wherein the amount of powdered active carbon is added during the FILL and/or REACT steps and is sufficient to produce a final effluent free of dioxins and PCB's containing less than 0.8 ppt and less than 2.0 ppb, respectively, and substantially free of other halogenated organic compounds, and disposing of waste sludge in a secure landfill.

  9. Sorption of toxic organic compounds on waste-water solids: Correlation with fundamental properties

    SciTech Connect

    Dobbs, R.A.; Wang, L.; Govind, R.

    1989-01-01

    Sorption of toxic organic compounds on primary, mixed-liquor, and digested solids from municipal waste-water treatment plants was correlated with octanol/water partition coefficients and with modified Randic indexes. The correlations developed are useful for assessing the role of sorption in the treatment of toxic or hazardous compounds in conventional biological waste-water treatment plants. Correlations developed provide a basis for predicting the concentration of toxic compounds associated with waste-water solids at a given equilibrium concentration in the aqueous phase. Organics in sludge can impact anaerobic digestion, land spreading, incineration and ocean dumping of sludges. Estimates of the concentration of toxics in sludge allows assessment of the impact of toxics on sludge-disposal options.

  10. MICROBIAL REMOVAL OF WASTEWATER ORGANIC COMPOUNDS AS A FUNCTION OF INPUT CONCENTRATION IN SOIL COLUMNS

    EPA Science Inventory

    The fate of six organic compounds during rapid infiltration of primary wastewater through soil columns was studied. Breakthrough profiles of o-phenylphenol were relatively consistent during the test, with fractional breakthrough (mass output/mass input) being independent of input...

  11. Organic Wastewater Compounds, Pharmaceuticals, andColiphage in Ground Water Receiving Discharge from OnsiteWastewater Treatment Systems near La Pine, Oregon:Occurrence and Implications for Transport

    USGS Publications Warehouse

    Hinkle, Stephen J.; Weick, Rodney J.; Johnson, Jill M.; Cahill, Jeffery D.; Smith, Steven G.; Rich, Barbara J.

    2005-01-01

    The occurrence of organic wastewater compounds (components of 'personal care products' and other common household chemicals), pharmaceuticals (human prescription and nonprescription medical drugs), and coliphage (viruses that infect coliform bacteria, and found in high concentrations in municipal wastewater) in onsite wastewater (septic tank effluent) and in a shallow, unconfined, sandy aquifer that serves as the primary source of drinking water for most residents near La Pine, Oregon, was documented. Samples from two types of observation networks provided basic occurrence data for onsite wastewater and downgradient ground water. One observation network was a group of 28 traditional and innovative (advanced treatment) onsite wastewater treatment systems and associated downgradient drainfield monitoring wells, referred to as the 'innovative systems network'. The drainfield monitoring wells were located adjacent to or under onsite wastewater treatment system drainfield lines. Another observation network, termed the 'transect network', consisted of 31 wells distributed among three transects of temporary, stainless-steel-screened, direct-push monitoring wells installed along three plumes of onsite wastewater. The transect network, by virtue of its design, also provided a basis for increased understanding of the transport of analytes in natural systems. Coliphage were frequently detected in onsite wastewater. Coliphage concentrations in onsite wastewater were highly variable, ranging from less than 1 to 3,000,000 plaque forming units per 100 milliliters. Coliphage were occasionally detected (eight occurrences) at low concentrations in samples from wells located downgradient from onsite wastewater treatment system drainfield lines. However, coliphage concentrations were below method detection limits in replicate or repeat samples collected from the eight sites. The consistent absence of coliphage detections in the replicate or repeat samples is interpreted to indicate that the detections reported for ground-water samples represented low-level field or laboratory contamination, and it would appear that coliphage were effectively attenuated to less than 1 PFU/100 mL over distances of several feet of transport in the La Pine aquifer and (or) overlying unsaturated zone. Organic wastewater compounds were frequently detected in onsite wastewater. Of the 63 organic wastewater compounds in the analytical schedule, 45 were detected in the 21 samples of onsite wastewater. Concentrations of organic wastewater compounds reached a maximum of 1,300 ug/L (p-cresol). Caffeine was detected at concentrations as high as 320 ug/L. Fourteen of the 45 compounds were detected in more than 90 percent of onsite wastewater samples. Fewer (nine) organic wastewater compounds were detected in ground water, despite the presence of nitrate and chloride likely from onsite wastewater sources. The nine organic wastewater compounds that were detected in ground-water samples were acetyl-hexamethyl-tetrahydro-naphthalene (AHTN), caffeine, cholesterol, hexahydrohexamethyl-cyclopentabenzopyran, N,N-diethyl-meta-toluamide (DEET), tetrachloroethene, tris (2-chloroethyl) phosphate, tris (dichloroisopropyl) phosphate, and tributyl phosphate. Frequent detection of household-chemical type organic wastewater compounds in onsite wastewater provides evidence that some of these organic wastewater compounds may be useful indicators of human waste effluent dispersal in some hydrologic environments. The occurrence of organic wastewater compounds in ground water downgradient from onsite wastewater treatment systems demonstrates that a subgroup of organic wastewater compounds is transported in the La Pine aquifer. The consistently low concentrations (generally less than 1 ug/L) of organic wastewater compounds in water samples collected from wells located no more than 19 feet from drainfield lines indicates that the reactivity (sorption, degradation) of this suite of organic waste

  12. Production of a High Efficiency Microbial Flocculant by Proteus mirabilis TJ-1 Using Compound Organic Wastewater

    NASA Astrophysics Data System (ADS)

    Zhang, Zhiqiang; Xia, Siqing; Zhang, Jiao

    2010-11-01

    The production of a high efficiency microbial flocculant (MBF) by Proteus mirabilis TJ-1 using compound organic wastewater was investigated. To cut down the cost of the MBF production, several nutritive organic wastewaters were selected to replace glucose and peptone as the carbon source and the nitrogen source in the optimized medium of strain TJ-1, respectively. The compound wastewater of the milk candy and the soybean milk was found to be good carbon source and nitrogen source for this strain to produce MBF. The cost-effective culture medium consists of (per liter): 800 mL wastewater of milk candy, 200 mL wastewater of soybean milk, 0.3 g MgSO4?7 H2O, 5 g K2HPO4, 2 g and KH2PO4, pH 7.0. The economic cost for the MBF production can be cut down over a half by using the developed culture medium. Furthermore, the utilization of the two wastewaters in the preparation of culture medium of strain TJ-1 can not only save their big treatment cost, but also realize their resource reuse.

  13. Occurrence of pharmaceuticals, hormones, and organic wastewater compounds in Pennsylvania waters, 2006-09

    USGS Publications Warehouse

    Reif, Andrew G.; Crawford, J. Kent; Loper, Connie A.; Proctor, Arianne; Manning, Rhonda; Titler, Robert

    2012-01-01

    Concern over the presence of contaminants of emerging concern, such as pharmaceutical compounds, hormones, and organic wastewater compounds (OWCs), in waters of the United States and elsewhere is growing. Laboratory techniques developed within the last decade or new techniques currently under development within the U.S. Geological Survey now allow these compounds to be measured at concentrations in nanograms per liter. These new laboratory techniques were used in a reconnaissance study conducted by the U.S. Geological Survey, in cooperation with the Pennsylvania Department of Environmental Protection, to determine the occurrence of contaminants of emerging concern in streams, streambed sediment, and groundwater of Pennsylvania. Compounds analyzed for in the study are pharmaceuticals (human and veterinary drugs), hormones (natural and synthetic), and OWCs (detergents, fragrances, pesticides, industrial compounds, disinfectants, polycyclic aromatic hydrocarbons, fire retardants and plasticizers). Reconnaissance sampling was conducted from 2006 to 2009 to identify contaminants of emerging concern in (1) groundwater from wells used to supply livestock, (2) streamwater upstream and downstream from animal feeding operations, (3) streamwater upstream from and streamwater and streambed sediment downstream from municipal wastewater effluent discharges, (4) streamwater from sites within 5 miles of drinking-water intakes, and (5) streamwater and streambed sediment where fish health assessments were conducted. Of the 44 pharmaceutical compounds analyzed in groundwater samples collected in 2006 from six wells used to supply livestock, only cotinine (a nicotine metabolite) and the antibiotics tylosin and sulfamethoxazole were detected. The maximum concentration of any contaminant of emerging concern was 24 nanograms per liter (ng/L) for cotinine, and was detected in a groundwater sample from a Lebanon County, Pa., well. Seven pharmaceutical compounds including acetaminophen, caffeine, carbamazepine, and the four antibiotics tylosin, sulfadimethoxine, sulfamethoxazole, and oxytetracycline were detected in streamwater samples collected in 2006 from six paired stream sampling sites located upstream and downstream from animal-feeding operations. The highest reported concentration of these seven compounds was for the antibiotic sulfamethoxazole (157 ng/L), in a sample from the downstream site on Snitz Creek in Lancaster County, Pa. Twenty-one pharmaceutical compounds were detected in streamwater samples collected in 2006 from five paired stream sampling sites located upstream or downstream from a municipal wastewater-effluent-discharge site. The most commonly detected compounds and maximum concentrations were the anticonvulsant carbamazepine, 276 ng/L; the antihistamine diphenhydramine, 135 ng/L; and the antibiotics ofloxacin, 329 ng/L; sulfamethoxazole, 1,340 ng/L; and trimethoprim, 256 ng/L. A total of 51 different contaminants of emerging concern were detected in streamwater samples collected from 2007 through 2009 at 13 stream sampling sites located downstream from a wastewater-effluent-discharge site. The concentrations and numbers of compounds detected were higher in stream sites downstream from a wastewater-effluent-discharge site than in stream sites upstream from a wastewater-effluent-discharge site. This finding indicates that wastewater-effluent discharges are a source of contaminants of emerging concern; these contaminants were present more frequently in the streambed-sediment samples than in streamwater samples. Antibiotic compounds were often present in both the streamwater and streambed-sediment samples, but many OWCs were present exclusively in the streambed-sediment samples. Compounds with endocrine disrupting potential including detergent metabolites, pesticides, and flame retardants, were present in the streamwater and streambed-sediment samples. Killinger Creek, a stream where wastewater-effluent discharges contribute a large percentage of the total flow, stands out as a stream with particularly high numbers of compound

  14. Membrane filtration of agro-industrial wastewaters and isolation of organic compounds with high added values.

    PubMed

    Zagklis, Dimitris P; Paraskeva, Christakis A

    2014-01-01

    The aim of the current study was the exploitation of agro-industrial wastes or by-products such as olive mill wastewater (OMW) and defective wines. A cost-effective system for their maximum exploitation is suggested, using a combined process of membrane filtration and other physicochemical processes. Wastewaters are first treated in a membrane system (prefiltration, ultrafiltration, nanofiltration, and reverse osmosis) where pure water and other organic fractions (by-products) are obtained. Organic fractions, called hereafter byproducts and not wastes, are further treated for the separation of organic compounds and isolation of high added value products. Experiments were performed with OMW and defective wines as characteristic agro-industrial wastewaters. Profit from the exploitation of agro-industrial wastewaters can readily help the depreciation of the indeed high cost process of membrane filtration. The simple phenolic fraction of the OMW was successfully isolated from the rest of the waste, and problems occurring during winemaking, such as high volatile acidity and odours, were tackled. PMID:24434988

  15. Simultaneous removal of inorganic and organic compounds in wastewater by freshwater green microalgae.

    PubMed

    Zhou, Guang-Jie; Ying, Guang-Guo; Liu, Shan; Zhou, Li-Jun; Chen, Zhi-Feng; Peng, Fu-Qiang

    2014-08-01

    Batch experiments were carried out for 7 days to investigate the simultaneous removal of various organic and inorganic contaminants including total nitrogen (TN), total phosphorus (TP), metals, pharmaceuticals and personal care products (PPCPs), endocrine disrupting chemicals (EDCs), and estrogenic activity in wastewater by four freshwater green microalgae species, Chlamydomonas reinhardtii, Scenedesmus obliquus, Chlorella pyrenoidosa and Chlorella vulgaris. After treatment for 7 days, 76.7-92.3% of TN, and 67.5-82.2% of TP were removed by these four algae species. The removal of metals from wastewater by the four algae species varied among the metal species. These four algae species could remove most of the metals efficiently (>40% removal), but showed low efficiencies in removing Pb, Ni and Co. The four algae species were also found to be efficient in removing most of the selected organic compounds with >50% removal, and the estrogenic activity with removal efficiencies ranging from 46.2 to 81.1% from the wastewater. Therefore, algae could be harnessed to simultaneously remove various contaminants in wastewater. PMID:24953257

  16. [Source emission characteristics and impact factors of volatile halogenated organic compounds from wastewater treatment plant].

    PubMed

    He, Jie; Wang, Bo-Guang; Liu, Shu-Le; Zhao, De-Jun; Tang, Xiao-Dong; Zou, Yu

    2011-12-01

    A low enrichment method of using Tenax as absorbent and liquid nitrogen as refrigerant has been established to sample the volatile halogenated organic compounds in Guangzhou Liede municipal wastewater treatment plant as well as its ambient air. The composition and concentration of target halogenated hydrocarbons were analyzed by combined thermal desorption/GC-MS to explore its sources profile and impact factors. The result showed that 19 halogenated organic compounds were detected, including 11 halogenated alkanets, 3 halogenated alkenes, 3 halogenated aromatic hydrocarbons and 2 haloesters, with their total concentrations ranged from 34.91 microg x m(-3) to 127.74 microg x m(-3) and mean concentrations ranged from n.d. to 33.39 microg x m(-3). Main pollutants of the studied plant were CH2Cl2, CHCl3, CFC-12, C2H4Cl2, CFC-11, C2HCl3 and C2Cl4, they came from the wastewater by volatilization. Among the six processing units, the dehydration room showed the highest level of halogenated organic compounds, followed by pumping station, while the sludge thickener was the lowest. The emissions from pumping station, aeration tank and biochemical pool were significantly affected by temperature and humidity of environment. PMID:22468521

  17. Sorption interactions of organic compounds with soils affected by agricultural olive mill wastewater.

    PubMed

    Keren, Yonatan; Borisover, Mikhail; Bukhanovsky, Nadezhda

    2015-11-01

    The organic compound-soil interactions may be strongly influenced by changes in soil organic matter (OM) which affects the environmental fate of multiple organic pollutants. The soil OM changes may be caused by land disposal of various OM-containing wastes. One unique type of OM-rich waste is olive mill-related wastewater (OMW) characterized by high levels of OM, the presence of fatty aliphatics and polyphenolic aromatics. The systematic data on effects of the land-applied OMW on organic compound-soil interactions is lacking. Therefore, aqueous sorption of simazine and diuron, two herbicides, was examined in batch experiments onto three soils, including untreated and OMW-affected samples. Typically, the organic compound-soil interactions increased following the prior land application of OMW. This increase is associated with the changes in sorption mechanisms and cannot be attributed solely to the increase in soil organic carbon content. A novel observation is that the OMW application changes the soil-sorbent matrix in such a way that the solute uptake may become cooperative or the existing ability of a soil sorbent to cooperatively sorb organic molecules from water may become characterized by a larger affinity. The remarkable finding of this study was that in some cases a cooperative uptake of organic molecules by soils makes itself evident in distinct sigmoidal sorption isotherms rarely observed in soil sorption of non-ionized organic compounds; the cooperative herbicide-soil interactions may be characterized by the Hill model coefficients. However, no single trend was found for the effect of applied OMW on the mechanisms of organic compound-soil interactions. PMID:26183941

  18. Fate of trace organic compounds during vadose zone soil treatment in an onsite wastewater system

    USGS Publications Warehouse

    Conn, K.E.; Siegrist, R.L.; Barber, L.B.; Meyer, M.T.

    2010-01-01

    During onsite wastewater treatment, trace organic compounds are often present in the effluents applied to subsurface soils for advanced treatment during vadose zone percolation and groundwater recharge. The fate of the endocrine-disrupting surfactant metabolites 4-nonylphenol (NP), 4-nonylphenolmonoethoxylate (NP1EO), and 4-nonylphenolmonoethoxycarboxylate (NP1EC), metal-chelating agents ethylenediaminetetraacetic acid (EDTA) and nitrilotriacetic acid (NTA), antimicrobial agent triclosan, stimulant caffeine, and antibiotic sulfamethoxazole during transport through an unsaturated sandy loam soil was studied at a field-scale test site. To assess the effects of effluent quality and hydraulic loading rate (HLR) on compound fate in the soil profile, two effluents (septic tank or textile biofilter) were applied at two design HLRs (2 or 8 cm/d). Chemical concentrations were determined in the two effluents and soil pore water at 60, 120, and 240 cm below the soil infiltrative surface. Concentrations of trace organic compounds in septic tank effluent were reduced by more than 90% during transport through 240 cm (often within 60 cm) of soil, likely due to sorption and biotransformation. However, the concentration of NP increased with depth in the shallow soil profile. Additional treatment of anaerobic septic tank effluent with an aerobic textile biofilter reduced effluent concentrations of many compounds, but generally did not affect any changes in pore water concentrations. The soil profile receiving septic tank effluent (vs. textile biofilter effluent) generally had greater percent removal efficiencies. EDTA, NP, NP1EC, and sulfamethoxazole were measured in soil pore water, indicating the ability of some trace organic compounds to reach shallow groundwater. Risk is highly dependent on the degree of further treatment in the saturated zone and the types and proximity of uses for the receiving groundwater environment. ?? 2009 SETAC.

  19. Analysis of pharmaceutical and other organic wastewater compounds in filtered and unfiltered water samples by gas chromatography/mass spectrometry

    USGS Publications Warehouse

    Zaugg, Steven D.; Phillips, Patrick; Smith, Steven G.

    2014-01-01

    Research on the effects of exposure of stream biota to complex mixtures of pharmaceuticals and other organic compounds associated with wastewater requires the development of additional analytical capabilities for these compounds in water samples. Two gas chromatography/mass spectrometry (GC/MS) analytical methods used at the U.S. Geological Survey National Water Quality Laboratory (NWQL) to analyze organic compounds associated with wastewater were adapted to include additional pharmaceutical and other organic compounds beginning in 2009. This report includes a description of method performance for 42 additional compounds for the filtered-water method (hereafter referred to as the filtered method) and 46 additional compounds for the unfiltered-water method (hereafter referred to as the unfiltered method). The method performance for the filtered method described in this report has been published for seven of these compounds; however, the addition of several other compounds to the filtered method and the addition of the compounds to the unfiltered method resulted in the need to document method performance for both of the modified methods. Most of these added compounds are pharmaceuticals or pharmaceutical degradates, although two nonpharmaceutical compounds are included in each method. The main pharmaceutical compound classes added to the two modified methods include muscle relaxants, opiates, analgesics, and sedatives. These types of compounds were added to the original filtered and unfiltered methods largely in response to the tentative identification of a wide range of pharmaceutical and other organic compounds in samples collected from wastewater-treatment plants. Filtered water samples are extracted by vacuum through disposable solid-phase cartridges that contain modified polystyrene-divinylbenzene resin. Unfiltered samples are extracted by using continuous liquid-liquid extraction with dichloromethane. The compounds of interest for filtered and unfiltered sample types were determined by use of the capillary-column gas chromatography/mass spectrometry. The performance of each method was assessed by using data on recoveries of compounds in fortified surface-water, wastewater, and reagent-water samples. These experiments (referred to as spike experiments) consist of fortifying (or spiking) samples with known amounts of target analytes. Surface-water-spike experiments were performed by using samples obtained from a stream in Colorado (unfiltered method) and a stream in New York (filtered method). Wastewater spike experiments for both the filtered and unfiltered methods were performed by using a treated wastewater obtained from a single wastewater treatment plant in New York. Surface water and wastewater spike experiments were fortified at both low and high concentrations and termed low- and high-level spikes, respectively. Reagent water spikes were assessed in three ways: (1) set spikes, (2) a low-concentration fortification experiment, and (3) a high-concentration fortification experiment. Set spike samples have been determined since 2009, and consist of analysis of fortified reagent water for target compounds included for each group of 10 to18 environmental samples analyzed at the NWQL. The low-concentration and high-concentration reagent spike experiments, by contrast, represent a one-time assessment of method performance. For each spike experiment, mean recoveries ranging from 60 to 130 percent indicate low bias, and relative standard deviations (RSDs) less than ( Of the compounds included in the filtered method, 21 had mean recoveries ranging from 63 to 129 percent for the low-level and high-level surface-water spikes, and had low ()132 percent]. For wastewater spikes, 24 of the compounds included in the filtered method had recoveries ranging from 61 to 130 percent for the low-level and high-level spikes. RSDs were 130 percent) or variable recoveries (RSDs >30 percent) for low-level wastewater spikes, or low recoveries ( Of the compounds included in the unfiltered method, 17 had mean spike recoveries ranging from 74

  20. Volatile organic compound emissions from wastewater treatment plants in Taiwan: legal regulations and costs of control.

    PubMed

    Cheng, Wen-Hsi; Hsu, Shu-Kang; Chou, Ming-Shean

    2008-09-01

    This study assessed volatile organic compound (VOC) emission characteristics from wastewater treatment plants (WWTPs) in five Taiwanese industrial districts engaged in numerous manufacturing processes, including petrochemical, science-based industry (primarily semiconductors, photo-electronics, electronic products and biological technology), as well as multiple manufacturing processes (primarily pharmaceuticals and paint manufacturing). The most aqueous hydrocarbons dissolved in the wastewater of Taiwanese WWTPs were acetone, acrylonitrile, methylene chloride, and chloroform for the petrochemical districts; acetone, chloroform, and toluene for the science-based districts; and chlorinated and aromatic hydrocarbons for the multiple industrial districts. The aqueous pollutants in the united WWTPs were closely related to the characteristics of the manufacturing plants in the districts. To effectively prevent VOC emissions from the primary treatment section of petrochemical WWTPs, the updated regulations governing VOC emissions were issued by the Taiwanese Environmental Protection Administration in September 2005, legally mandating a seal cover system incorporating venting and air purification equipment. Cost analysis indicates that incinerators with regenerative heat recovery are optimal for treating high VOC concentrations, exceeding 10,000 ppm as CH(4), from the oil separation basins. However, the emission concentrations, ranging from 100 to 1,000 ppm as CH(4) from the other primary treatment facilities and bio-treatment stages, should be collected and then injected into the biological oxidation basins via existing or new blowers. The additional capital and operating costs required to treat the VOC emissions of 1,000 ppm as CH(4) from primary treatment facilities are less than USD 0.1 for per m(3) wastewater treatment capacity. PMID:17825475

  1. Microbial removal of wastewater organic compounds as a function of input concentration in soil columns.

    PubMed

    Hutchins, S R; Tomson, M B; Wilson, J T; Ward, C H

    1984-11-01

    The fate of six organic compounds during rapid infiltration of primary wastewater through soil columns was studied. Feed solutions were prepared which contained all six compounds in individual concentrations ranging from 1 to 1,000 micrograms/liter and were applied to separate soil columns on a flooding-drying schedule. Feed solutions and column effluents were analyzed for the compounds by XAD resin (Rohm and Haas Co.) extraction and gas chromatography-mass spectrometry during each of three successive inundation cycles. Breakthrough profiles of o-phenylphenol were relatively consistent during the test, with fractional breakthrough (mass output/mass input) being independent of input concentration. Consistent profiles were also observed for 2-(methylthio)benzothiazole, although fractional breakthroughs were higher at lower input concentrations, indicating that removal processes were operating less efficiently at these levels. The behavior of p-dichlorobenzene was similar to that of 2-(methylthio)benzothiazole after the first inundation cycle, with the exception that increased fractional breakthroughs were observed at the highest input concentration as well. Microbial adaptation was evident for benzophenone, 2-methylnaphthalene, and p-(1,1,3,3-tetramethylbutyl)phenol, as indicated by increased removal efficiencies during successive inundation cycles, especially at the higher input concentrations. Column effluent concentrations of the latter two compounds were independent of input concentrations during the final stage of the test. Microbial activity and adaptation were confirmed for several of the compounds by using isotopes and measuring the extent of mineralization in batch tests with soil from one of the columns.(ABSTRACT TRUNCATED AT 250 WORDS) PMID:6508302

  2. Pharmaceuticals, perfluorosurfactants, and other organic wastewater compounds in public drinking water wells in a shallow sand and gravel aquifer.

    PubMed

    Schaider, Laurel A; Rudel, Ruthann A; Ackerman, Janet M; Dunagan, Sarah C; Brody, Julia Green

    2014-01-15

    Approximately 40% of U.S. residents rely on groundwater as a source of drinking water. Groundwater, especially unconfined sand and gravel aquifers, is vulnerable to contamination from septic systems and infiltration of wastewater treatment plant effluent. In this study, we characterized concentrations of pharmaceuticals, perfluorosurfactants, and other organic wastewater compounds (OWCs) in the unconfined sand and gravel aquifer of Cape Cod, Massachusetts, USA, where septic systems are prevalent. Raw water samples from 20 public drinking water supply wells on Cape Cod were tested for 92 OWCs, as well as surrogates of wastewater impact. Fifteen of 20 wells contained at least one OWC; the two most frequently-detected chemicals were sulfamethoxazole (antibiotic) and perfluorooctane sulfonate (perfluorosurfactant). Maximum concentrations of sulfamethoxazole (113 ng/L) and the anticonvulsant phenytoin (66 ng/L) matched or exceeded maximum reported concentrations in other U.S. public drinking water sources. The sum of pharmaceutical concentrations and the number of detected chemicals were both significantly correlated with nitrate, boron, and extent of unsewered residential and commercial development within 500 m, indicating that wastewater surrogates can be useful for identifying wells most likely to contain OWCs. Septic systems appear to be the primary source of OWCs in Cape Cod groundwater, although wastewater treatment plants and other sources were potential contributors to several wells. These results show that drinking water supplies in unconfined aquifers where septic systems are prevalent may be among the most vulnerable to OWCs. The presence of mixtures of OWCs in drinking water raises human health concerns; a full evaluation of potential risks is limited by a lack of health-based guidelines and toxicity assessments. PMID:24055660

  3. A POLYMER-CERAMIC COMPOSITE MEMBRANE FOR RECOVERING VOLATILE ORGANIC COMPOUNDS FROM WASTEWATERS BY PERVAPORATION

    EPA Science Inventory

    A composite membrane was constructed on a porous ceramic support from a block copolymer of styrene and butadiene (SBS). It was tested in a laboratory pervaporation apparatus for recovering volatile organic compounds (VOCs) such a 1,1,1-trichloroethane (TCA) and trichloroethylene ...

  4. Occurrence of organic wastewater compounds in drinking water, wastewater effluent, and the Big Sioux River in or near Sioux Falls, South Dakota, 2001-2004

    USGS Publications Warehouse

    Sando, Steven K.; Furlong, Edward T.; Gray, James L.; Meyer, Michael T.

    2006-01-01

    The U.S. Geological Survey (USGS) in cooperation with the city of Sioux Falls conducted several rounds of sampling to determine the occurrence of organic wastewater compounds (OWCs) in the city of Sioux Falls drinking water and waste-water effluent, and the Big Sioux River in or near Sioux Falls during August 2001 through May 2004. Water samples were collected during both base-flow and storm-runoff conditions. Water samples were collected at 8 sites, which included 4 sites upstream from the wastewater treatment plant (WWTP) discharge, 2 sites downstream from the WWTP discharge, 1 finished drinking-water site, and 1 WWTP effluent (WWE) site. A total of 125 different OWCs were analyzed for in this study using five different analytical methods. Analyses for OWCs were performed at USGS laboratories that are developing and/or refining small-concentration (less than 1 microgram per liter (ug/L)) analytical methods. The OWCs were classified into six compound classes: human pharmaceutical compounds (HPCs); human and veterinary antibiotic compounds (HVACs); major agricultural herbicides (MAHs); household, industrial,and minor agricultural compounds (HIACs); polyaromatic hydrocarbons (PAHs); and sterol compounds (SCs). Some of the compounds in the HPC, MAH, HIAC, and PAH classes are suspected of being endocrine-disrupting compounds (EDCs). Of the 125 different OWCs analyzed for in this study, 81 OWCs had one or more detections in environmental samples reported by the laboratories, and of those 81 OWCs, 63 had acceptable analytical method performance, were detected at concentrations greater than the study reporting levels, and were included in analyses and discussion related to occurrence of OWCs in drinking water, wastewater effluent, and the Big Sioux River. OWCs in all compound classes were detected in water samples from sampling sites in the Sioux Falls area. For the five sampling periods when samples were collected from the Sioux Falls finished drinking water, only one OWC was detected at a concentration greater than the study reporting level (metolachlor; 0.0040 ug/L). During base-flow conditions, Big Sioux River sites upstream from the WWTP discharge had OWC contributions that primarily were from nonpoint animal or crop agriculture sources or had OWC concentrations that were minimal. The influence of the WWTP discharge on OWCs at downstream river sites during base-flow conditions ranged from minimal influence to substantial influence depending on the sampling period. During runoff conditions, OWCs at sites upstream from the WWTP discharge probably were primarily contributed by nonpoint animal and/or crop agriculture sources and possibly by stormwater runoff from nearby roads. OWCs at sites downstream from the WWTP discharge probably were contributed by sources other than the WWTP effluent discharge, such as stormwater runoff from urban and/or agriculture areas and/or resuspension of OWCs adsorbed to sediment deposited in the Big Sioux River. OWC loads generally were substantially smaller for upstream sites than downstream sites during both base-flow and runoff conditions.discharge had OWC contributions that primarily were from nonpoint animal or crop agriculture sources or had OWC concentrations that were minimal. The influence of the WWTP discharge on OWCs at downstream river sites during base-flow conditions ranged from minimal influence to substantial influence depending on the sampling period. During runoff conditions, OWCs at sites upstream from the WWTP discharge probably were primarily contributed by nonpoint animal and/or crop agriculture sources and possibly by stormwater runoff from nearby roads. OWCs at sites downstream from the WWTP discharge probably were contributed by sources other than the WWTP effluent discharge, such as stormwater runoff from urban and/or agriculture areas and/or resuspension of OWCs adsorbed to sediment deposited in the Big Sioux River. OWC loads generally were substantially smaller for

  5. Study of an organoclay for the sorption of dissolved organic compounds in the wastewaters from offshore platform operation.

    PubMed

    Scurtu, C; Leiknes, T; Helness, H

    2009-01-01

    The goal of this research work was to find a sorbent able to selectively retain the harmful dissolved compounds in the wastewaters from offshore platform operation but not the carboxylic acids and to study the effects of the most important parameters on the sorption process. BTX compounds (benzene, toluene and p-xylene) and acetic acid were chosen as the representatives of the harmful compounds and carboxylic acids groups respectively since they are found in the highest concentrations. An organically modified clay was determined to be the most suitable sorbent, where performance was evaluated at different values of pH (3, 5 and 8), acetic acid concentration (0, 160 and 320 mg/l), salinity (0, 35 and 70 g/l) and temperature (20, 40 and 60 degrees C). Results show that there is a sorption competition between BTX and acetic acid. Sorption of BTX compounds decreased with increasing initial acetic acid concentration and temperature, and increased proportionally with the salinity. Sorption of acetic acid, however, decreased with increasing pH, temperature and salinity. PMID:19403962

  6. Persistence of pharmaceutical compounds and other organic wastewater contaminants in a conventional drinking-water-treatment plant

    USGS Publications Warehouse

    Stackelberg, P.E.; Furlong, E.T.; Meyer, M.T.; Zaugg, S.D.; Henderson, A.K.; Reissman, D.B.

    2004-01-01

    In a study conducted by the US Geological Survey and the Centers for Disease Control and Prevention, 24 water samples were collected at selected locations within a drinking-water-treatment (DWT) facility and from the two streams that serve the facility to evaluate the potential for wastewater-related organic contaminants to survive a conventional treatment process and persist in potable-water supplies. Stream-water samples as well as samples of raw, settled, filtered, and finished water were collected during low-flow conditions, when the discharge of effluent from upstream municipal sewage-treatment plants accounted for 37-67% of flow in stream 1 and 10-20% of flow in stream 2. Each sample was analyzed for 106 organic wastewater-related contaminants (OWCs) that represent a diverse group of extensively used chemicals. Forty OWCs were detected in one or more samples of stream water or raw-water supplies in the treatment plant; 34 were detected in more than 10% of these samples. Several of these compounds also were frequently detected in samples of finished water; these compounds include selected prescription and non-prescription drugs and their metabolites, fragrance compounds, flame retardants and plasticizers, cosmetic compounds, and a solvent. The detection of these compounds suggests that they resist removal through conventional water-treatment processes. Other compounds that also were frequently detected in samples of stream water and raw-water supplies were not detected in samples of finished water; these include selected prescription and non-prescription drugs and their metabolites, disinfectants, detergent metabolites, and plant and animal steroids. The non-detection of these compounds indicates that their concentrations are reduced to levels less than analytical detection limits or that they are transformed to degradates through conventional DWT processes. Concentrations of OWCs detected in finished water generally were low and did not exceed Federal drinking-water standards or lifetime health advisories, although such standards or advisories have not been established for most of these compounds. Also, at least 11 and as many as 17 OWCs were detected in samples of finished water. Drinking-water criteria currently are based on the toxicity of individual compounds and not combinations of compounds. Little is known about potential human-health effects associated with chronic exposure to trace levels of multiple OWCs through routes such as drinking water. The occurrence in drinking-water supplies of many of the OWCs analyzed for during this study is unregulated and most of these compounds have not been routinely monitored for in the Nation's source- or potable-water supplies. This study provides the first documentation that many of these compounds can survive conventional water-treatment processes and occur in potable-water supplies. It thereby provides information that can be used in setting research and regulatory priorities and in designing future monitoring programs. The results of this study also indicate that improvements in water-treatment processes may benefit from consideration of the response of OWCs and other trace organic contaminants to specific physical and chemical treatments. ?? 2004 Elsevier B.V. All rights reserved.

  7. ANALYSIS OF CHLORINATED ORGANIC COMPOUNDS FORMED DURING CHLORINATION OF WASTEWATER PRODUCTS

    EPA Science Inventory

    Chemical byproducts produced during the chlorination of municipal wastewater were examined in a study that employed several specially modified analytical methodologies. Volatile byproducts were examined by the use of gas chromatography with selective detectors and gas chromatogra...

  8. THE EFFECT OF OZONATION OF ORGANICS IN WASTEWATER

    EPA Science Inventory

    The effect of ozone treatment of domestic wastewater and various model compounds has been determined with respect to trace organic components. Organic constituents were identified in wastewater that was treated with ozone at the Upper Thompson Sanitation District Treatment Plant,...

  9. Recycled water for stream flow augmentation: benefits, challenges, and the presence of wastewater-derived organic compounds.

    PubMed

    Plumlee, Megan H; Gurr, Christopher J; Reinhard, Martin

    2012-11-01

    Stream flow augmentation with recycled water has the potential to improve stream habitat and increase potable water supply, but the practice is not yet well understood or documented. The objectives of this report are to present a short review illustrated by a case study, followed by recommendations for future stream flow augmentation projects. Despite the fact that wastewater discharge to streams is commonplace, a water agency pursuing stream flow augmentation with recycled water will face unique challenges. For example, recycled water typically contains trace amounts of organic wastewater-derived compounds (OWCs) for which the potential ecological risks must be balanced against the benefits of an augmentation project. Successful stream flow augmentation with recycled water requires that the lead agency clearly articulate a strong project rationale and identify key benefits. It must be assumed that the public will have some concerns about water quality. Public acceptance may be better if an augmentation project has co-benefits beyond maintaining stream ecosystems, such as improving water system supply and reliability (i.e. potable use offset). Regulatory or project-specific criteria (acceptable concentrations of priority OWCs) would enable assessment of ecosystem impacts and demonstration of practitioner compliance. Additional treatment (natural or engineered) of the recycled water may be considered. If it is not deemed necessary or feasible, existing recycled water quality may be adequate to achieve project goals depending on project rationale, site and water quality evaluation, and public acceptance. PMID:23041295

  10. Predicting concentrations of trace organic compounds in municipal wastewater treatment plant sludge and biosolids using the PhATE™ model.

    PubMed

    Cunningham, Virginia L; D'Aco, Vincent J; Pfeiffer, Danielle; Anderson, Paul D; Buzby, Mary E; Hannah, Robert E; Jahnke, James; Parke, Neil J

    2012-07-01

    This article presents the capability expansion of the PhATE™ (pharmaceutical assessment and transport evaluation) model to predict concentrations of trace organics in sludges and biosolids from municipal wastewater treatment plants (WWTPs). PhATE was originally developed as an empirical model to estimate potential concentrations of active pharmaceutical ingredients (APIs) in US surface and drinking waters that could result from patient use of medicines. However, many compounds, including pharmaceuticals, are not completely transformed in WWTPs and remain in biosolids that may be applied to land as a soil amendment. This practice leads to concerns about potential exposures of people who may come into contact with amended soils and also about potential effects to plants and animals living in or contacting such soils. The model estimates the mass of API in WWTP influent based on the population served, the API per capita use, and the potential loss of the compound associated with human use (e.g., metabolism). The mass of API on the treated biosolids is then estimated based on partitioning to primary and secondary solids, potential loss due to biodegradation in secondary treatment (e.g., activated sludge), and potential loss during sludge treatment (e.g., aerobic digestion, anaerobic digestion, composting). Simulations using 2 surrogate compounds show that predicted environmental concentrations (PECs) generated by PhATE are in very good agreement with measured concentrations, i.e., well within 1 order of magnitude. Model simulations were then carried out for 18 APIs representing a broad range of chemical and use characteristics. These simulations yielded 4 categories of results: 1) PECs are in good agreement with measured data for 9 compounds with high analytical detection frequencies, 2) PECs are greater than measured data for 3 compounds with high analytical detection frequencies, possibly as a result of as yet unidentified depletion mechanisms, 3) PECs are less than analytical reporting limits for 5 compounds with low analytical detection frequencies, and 4) the PEC is greater than the analytical method reporting limit for 1 compound with a low analytical detection frequency, possibly again as a result of insufficient depletion data. Overall, these results demonstrate that PhATE has the potential to be a very useful tool in the evaluation of APIs in biosolids. Possible applications include: prioritizing APIs for assessment even in the absence of analytical methods; evaluating sludge processing scenarios to explore potential mitigation approaches; using in risk assessments; and developing realistic nationwide concentrations, because PECs can be represented as a cumulative probability distribution. Finally, comparison of PECs to measured concentrations can also be used to identify the need for fate studies of compounds of interest in biosolids. PMID:22162313

  11. Occurrence of Selected Pharmaceutical and Organic Wastewater Compounds in Effluent and Water Samples from Municipal Wastewater and Drinking-Water Treatment Facilities in the Tar and Cape Fear River Basins, North Carolina, 2003-2005

    USGS Publications Warehouse

    Ferrell, G.M.

    2009-01-01

    Samples of treated effluent and treated and untreated water were collected at 20 municipal wastewater and drinkingwater treatment facilities in the Tar and Cape Fear River basins of North Carolina during 2003 and 2005. The samples were analyzed for a variety of prescription and nonprescription pharmaceutical compounds and a suite of organic compounds considered indicative of wastewater. Concentrations of these compounds generally were less than or near the detection limits of the analytical methods used during this investigation. None of these compounds were detected at concentrations that exceeded drinking-water standards established by the U.S. Environmental Protection Agency. Bromoform, a disinfection byproduct, was the only compound detected at a concentration that exceeded regulatory guidelines. The concentration of bromoform in one finished drinking-water sample, 26 micrograms per liter, exceeded North Carolina water-quality criteria. Drinking-water treatment practices were effective at removing many of the compounds detected in untreated water. Disinfection processes used in wastewater treatment - chlorination or irradiation with ultraviolet light - did not seem to substantially degrade the organic compounds evaluated during this study.

  12. Organic contaminants in onsite wastewater treatment systems

    USGS Publications Warehouse

    Conn, K.E.; Siegrist, R.L.; Barber, L.B.; Brown, G.K.

    2007-01-01

    Wastewater from thirty onsite wastewater treatment systems was sampled during a reconnaissance field study to quantify bulk parameters and the occurrence of organic wastewater contaminants including endocrine disrupting compounds in treatment systems representing a variety of wastewater sources and treatment processes and their receiving environments. Bulk parameters ranged in concentrations representative of the wide variety of wastewater sources (residential vs. non-residential). Organic contaminants such as sterols, surfactant metabolites, antimicrobial agents, stimulants, metal-chelating agents, and other consumer product chemicals, measured by gas chromatography/mass spectrometry were detected frequently in onsite system wastewater. Wastewater composition was unique between source type likely due to differences in source water and chemical usage. Removal efficiencies varied by engineered treatment type and physicochemical properties of the contaminant, resulting in discharge to the soil treatment unit at ecotoxicologically-relevant concentrations. Organic wastewater contaminants were detected less frequently and at lower concentrations in onsite system receiving environments. Understanding the occurrence and fate of organic wastewater contaminants in onsite wastewater treatment systems will aid in minimizing risk to ecological and human health.

  13. Agricultural reuse of reclaimed water and uptake of organic compounds: pilot study at Mutah University wastewater treatment plant, Jordan.

    PubMed

    Al Nasir, Farah; Batarseh, Mufeed I

    2008-07-01

    The residues of polynuclear aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), chlorinated benzenes (CBs) and phenols were investigated for soil, wastewater, groundwater and plants. The uptake concentration of these compounds was comparatively determined using various plant types: Zea mays L., Helianthus annus L., Capsicum annum L., Abelmoschus esculentus L., Solanum melongena L. and Lycopersicon esculentum L. which were grown in a pilot site established at Mutah University wastewater treatment plant, Jordan. Soil, wastewater, groundwater and various plant parts (roots, leaves and fruits) samples were extracted in duplicate, cleaned up by open-column chromatography and analyzed by a multi-residue analytical methods using gas chromatography equipped with either mass selective detector (GC/MS), electron capture detector (GC/ECD), or flame ionization detector (FID). Environmentally relevant concentrations of targeted compounds were detected for wastewater much higher than for groundwater. The overall distribution profiles of PAHs and PCBs appeared similar for groundwater and wastewater indicating common potential pollution sources. The concentrations of PAHs, PCBs and phenols for different soils ranged from 169.34 to 673.20 microg kg(-1), 0.04 to 73.86 microg kg(-1) and 73.83 to 8724.42 microg kg(-1), respectively. However, much lower concentrations were detected for reference soil. CBs were detected in very low concentrations. Furthermore, it was found that different plants have different uptake and translocation behavior. As a consequence, there are some difficulties in evaluating the translocation of PAHs, CBs, PCBs and phenols from soil-roots-plant system. The uptake concentrations of various compounds from soil, in which plants grown, were dependent on plant variety and plant part, and they showed different uptake concentrations. Among the different plant parts, roots were found to be the most contaminated and fruits the least contaminated. PMID:18471853

  14. Occurrence and potential transport of selected pharmaceuticals and other organic wastewater compounds from wastewater-treatment plant influent and effluent to groundwater and canal systems in Miami-Dade County, Florida

    USGS Publications Warehouse

    Foster, Adam L.; Katz, Brian G.; Meyer, Michael T.

    2012-01-01

    An increased demand for fresh groundwater resources in South Florida has prompted Miami-Dade County to expand its water reclamation program and actively pursue reuse plans for aquifer recharge, irrigation, and wetland rehydration. The U.S. Geological Survey, in cooperation with the Miami-Dade Water and Sewer Department (WASD) and the Miami-Dade Department of Environmental Resources Management (DERM), initiated a study in 2008 to assess the presence of selected pharmaceuticals and other organic wastewater compounds in the influent and effluent at three regional wastewater-treatment plants (WWTPs) operated by the WASD and at one WWTP operated by the City of Homestead, Florida (HSWWTP).

  15. Relation between organic-wastewater compounds, groundwater geochemistry, and well characteristics for selected wells in Lansing, Michigan

    USGS Publications Warehouse

    Haack, Sheridan K.; Luukkonen, Carol L.

    2013-01-01

    In 2010, groundwater from 20 Lansing Board of Water and Light (BWL) production wells was tested for 69 organic-wastewater compounds (OWCs). The OWCs detected in one-half of the sampled wells are widely used in industrial and environmental applications and commonly occur in many wastes and stormwater. To identify factors that contribute to the occurrence of these constituents in BWL wells, the U.S. Geological Survey (USGS) interpreted the results of these analyses and related detections of OWCs to local characteristics and groundwater geochemistry. Analysis of groundwater-chemistry data collected by the BWL during routine monitoring from 1969 to 2011 indicates that the geochemistry of the BWL wells has changed over time, with the major difference being an increase in sodium and chloride. The concentrations of sodium and chloride were positively correlated to frequency of OWC detections. The BWL wells studied are all completed in the Saginaw aquifer, which consists of water-bearing sandstones of Pennsylvanian age. The Saginaw aquifer is underlain by the Parma-Bayport aquifer, and overlain by the Glacial aquifer. Two possible sources of sodium and chloride were evaluated: basin brines by way of the Parma-Bayport aquifer, and surficial sources by way of the Glacial aquifer. To determine if water from the underlying aquifer had influenced well-water geochemistry over time, the total dissolved solids concentration and changes in major ion concentrations were examined with respect to well depth, age, and pumping rate. To address a possible surficial source of sodium and chloride, 25 well, aquifer, or hydrologic characteristics, and 2 groundwater geochemistry variables that might influence whether, or the rate at which, water from the land surface could reach each well were compared to OWC detections and well chemistry. The statistical tests performed during this study, using available variables, indicated that reduced time of travel of water from the land surface to the well opening was significantly correlated with detections of OWCs. No specific well or aquifer characteristic was correlated with OWC detections; however, wells with detections tended to have less modeled confining material thickness (as simulated in the regional groundwater flow model), which is an estimate of the amount of clay or shale between the Glacial and Saginaw aquifers. Additional analyses and collection of other data would be required to more conclusively identify the source and to determine the potential vulnerability of other wells because each BWL well may have a somewhat unique set of characteristics that governs its response to pumping. Therefore, it is possible that a relevant explanatory variable was not included in this analysis. The current patterns of geochemistry, and the relation between these patterns and volume of pumpage for the BWL wells, indicates other wells may be susceptible to OWCs in the future.

  16. Design and evaluation of a field study on the contamination of selected volatile organic compounds and wastewater-indicator compounds in blanks and groundwater samples

    USGS Publications Warehouse

    Thiros, Susan A.; Bender, David A.; Mueller, David K.; Rose, Donna L.; Olsen, Lisa D.; Martin, Jeffrey D.; Bernard, Bruce; Zogorski, John S.

    2011-01-01

    The Field Contamination Study (FCS) was designed to determine the field processes that tend to result in clean field blanks and to identify potential sources of contamination to blanks collected in the field from selected volatile organic compounds (VOCs) and wastewater-indicator compounds (WICs). The VOCs and WICs analyzed in the FCS were detected in blanks collected by the U.S. Geological Survey (USGS) National Water-Quality Assessment (NAWQA) Program during 1996-2008 and 2002-08, respectively. To minimize the number of variables, the study required ordering of supplies just before sampling, storage of supplies and equipment in clean areas, and use of adequate amounts of purge-and-trap volatile-grade methanol and volatile pesticide-grade blank water (VPBW) to clean sampling equipment and to collect field blanks. Blanks and groundwater samples were collected during 2008-09 at 16 sites, which were a mix of water-supply and monitoring wells, located in 9 States. Five different sample types were collected for the FCS at each site: (1) a source-solution blank collected at the USGS National Water Quality Laboratory (NWQL) using laboratory-purged VPBW, (2) source-solution blanks collected in the field using laboratory-purged VPBW, (3) source-solution blanks collected in the field using field-purged VPBW, (4) a field blank collected using field-purged VPBW, and (5) a groundwater sample collected from a well. The source-solution blank and field-blank analyses were used to identify, quantify, and document extrinsic contamination and to help determine the sources and causes of data-quality problems that can affect groundwater samples. Concentrations of compounds detected in FCS analyses were quantified and results were stored in the USGS National Water Information System database after meeting rigorous identification and quantification criteria. The study also utilized information provided by laboratory analysts about evidence indicating the presence of selected compounds, using less rigorous identification criteria than is required for reporting data to the National Water Information System database. For the FCS, these data are considered adequate to indicate 'evidence of presence,' and were used only for diagnostic purposes. Evidence of VOCs and WICs at low concentrations near or less than the long-term method detection level can indicate a contamination problem that could affect future datasets if method detection levels were ever to be lowered. None of the 13 VOCs and 16 WICs included in this study were quantified in the VPBW collected and analyzed at the NWQL. This finding indicates that the VPBW was 'contaminant free' when it was shipped from the laboratory to each of the field offices, although some compounds were present in some of the samples at concentrations less than minimum detection levels based on evidence-of-presence data. Toluene, m- and p-xylene, benzene, and carbon disulfide were each quantified in an FCS field-blank analysis, but not in the associated groundwater sample. The native-water rinse of the sampling equipment conducted just before collection of the groundwater sample likely reduced low-level contamination with respect to these compounds. VOCs had lower detection frequencies in source-solution blanks and field blanks collected during the FCS than in the historical dataset collected by the NAWQA Program during 1996-2008. The detection frequency of toluene in field blanks was reduced about an order of magnitude from about 38 percent in the historical NAWQA dataset to 3.1 percent in the FCS dataset. Other VOCs quantified in 5 percent or more of the field blanks in the NAWQA dataset, but not quantified in the FCS field-blank analyses, were ethylbenzene, o-xylene, styrene, 1,2,4-trimethylbenzene, chloroform, dichloromethane, acetone, 2-butanone, and tetrahydrofuran. The lower detection frequencies of most VOCs for the FCS, compared to historical NAWQA data, can most likely be attributed to the use

  17. Occurrence of Selected Pharmaceuticals, Personal-Care Products, Organic Wastewater Compounds, and Pesticides in the Lower Tallapoosa River Watershed near Montgomery, Alabama, 2005

    USGS Publications Warehouse

    Oblinger, Carolyn J.; Gill, Amy C.; McPherson, Ann K.; Meyer, Michael T.; Furlong, Edward T.

    2007-01-01

    Synthetic and natural organic compounds derived from agricultural operations, residential development, and treated and untreated sanitary and industrial wastewater discharges can contribute contaminants to surface and ground waters. To determine the occurrence of these compounds in the lower Tallapoosa River watershed, Alabama, new laboratory methods were used that can detect human and veterinary antibiotics; pharmaceuticals; and compounds found in personal-care products, food additives, detergents and their metabolites, plasticizers, and other industrial and household products in the environment. Well-established methods for detecting 47 pesticides and 19 pesticide degradates also were used. In all, 186 different compounds were analyzed by using four analytical methods. The lower Tallapoosa River serves as the water-supply source for more than 100,000 customers of the Montgomery Water Works and Sanitary Sewer Board. Source-water protection is a high priority for the Board, which is responsible for providing safe drinking water. The U.S. Geological Survey, in cooperation with the Montgomery Water Works and Sanitary Sewer Board, conducted this study to provide baseline data that could be used to assess the effects of agriculture and residential development on the occurrence of selected organic compounds in the lower Tallapoosa River watershed. Twenty samples were collected at 10 sites on the Tallapoosa River and its tributaries. Ten samples were collected in April 2005 during high base streamflow, and 10 samples were collected in October 2005 when base streamflow was low. Thirty-two of 186 compounds were detected in the lower Tallapoosa River watershed. Thirteen compounds, including atrazine, 2-chloro-4-isopropylamino-6-amino-s-triazine (CIAT), hexazinone, metalaxyl, metolachlor, prometryn, prometon, simazine, azithromycin, oxytetracycline, sulfamethoxazole, trimethoprim, and tylosin, had measurable concentrations above their laboratory reporting levels. Concentrations were estimated for an additional 19 compounds that were detected below their laboratory reporting levels. The two most frequently detected compounds were the pesticides atrazine (19 of 20 samples) and simazine (13 of 20 samples). Tylosin, a veterinary antibiotic, was detected in 8 of 20 samples. Other compounds frequently detected at very low concentrations included CIAT and hexazinone (a degradate of atrazine and a pesticide, respectively); camphor (derived from personal-care products or flavorants), para-cresol (various uses including solvent, wood preservative, and in household cleaning products), and N,N-diethyl-m-toluamide (DEET, an insect repellent).

  18. Changes in reproductive biomarkers in an endangered fish species (bonytail chub, Gila elegans) exposed to low levels of organic wastewater compounds in a controlled experiment

    USGS Publications Warehouse

    Walker, David B.; Paretti, Nicholas V.; Cordy, Gail; Gross, Timothy S.; Zaugg, Steven D.; Furlong, Edward T.; Kolpin, Dana W.; Matter, William J.; Gwinn, Jessica; McIntosh, Dennis

    2009-01-01

    In arid regions of the southwestern United States, municipal wastewater treatment plants commonly discharge treated effluent directly into streams that would otherwise be dry most of the year. A better understanding is needed of how effluent-dependent waters (EDWs) differ from more natural aquatic ecosystems and the ecological effect of low levels of environmentally persistent organic wastewater compounds (OWCs) with distance from the pollutant source. In a controlled experiment, we found 26 compounds common to municipal effluent in treatment raceways all at concentrations <1.0 ?g/L. Male bonytail chub (Gila elegans) in tanks containing municipal effluent had significantly lower levels of 11-ketotestosterone (p = 0.021) yet higher levels of 17?-estradiol (p = 0.002) and vitellogenin (p = 0.036) compared to control male fish. Female bonytail chub in treatment tanks had significantly lower concentrations of 17?-estradiol than control females (p = 0.001). The normally inverse relationship between primary male and female sex hormones, expected in un-impaired fish, was greatly decreased in treatment (r = 0.00) versus control (r = ?0.66) female fish. We found a similar, but not as significant, trend between treatment (r = ?0.45) and control (r = ?0.82) male fish. Measures of fish condition showed no significant differences between male or female fish housed in effluent or clean water. Inter-sex condition did not occur and testicular and ovarian cells appeared normal for the respective developmental stage and we observed no morphological alteration in fish. The population-level impacts of these findings are uncertain. Studies examining the long-term, generational and behavioral effects to aquatic organisms chronically exposed to low levels of OWC mixtures are needed.

  19. Changes in reproductive biomarkers in an endangered fish species (bonytail chub, Gila elegans) exposed to low levels of organic wastewater compounds in a controlled experiment

    USGS Publications Warehouse

    Walker, D.B.; Paretti, N.V.; Cordy, G.; Gross, T.S.; Zaugg, S.D.; Furlong, E.T.; Kolpin, D.W.; Matter, W.J.; Gwinn, J.; McIntosh, D.

    2009-01-01

    In arid regions of the southwestern United States, municipal wastewater treatment plants commonly discharge treated effluent directly into streams that would otherwise be dry most of the year. A better understanding is needed of how effluent-dependent waters (EDWs) differ from more natural aquatic ecosystems and the ecological effect of low levels of environmentally persistent organic wastewater compounds (OWCs) with distance from the pollutant source. In a controlled experiment, we found 26 compounds common to municipal effluent in treatment raceways all at concentrations <1.0 ??g/L. Male bonytail chub (Gila elegans) in tanks containing municipal effluent had significantly lower levels of 11-ketotestosterone (p = 0.021) yet higher levels of 17??-estradiol (p = 0.002) and vitellogenin (p = 0.036) compared to control male fish. Female bonytail chub in treatment tanks had significantly lower concentrations of 17??-estradiol than control females (p = 0.001). The normally inverse relationship between primary male and female sex hormones, expected in un-impaired fish, was greatly decreased in treatment (r = 0.00) versus control (r = -0.66) female fish. We found a similar, but not as significant, trend between treatment (r = -0.45) and control (r = -0.82) male fish. Measures of fish condition showed no significant differences between male or female fish housed in effluent or clean water. Inter-sex condition did not occur and testicular and ovarian cells appeared normal for the respective developmental stage and we observed no morphological alteration in fish. The population-level impacts of these findings are uncertain. Studies examining the long-term, generational and behavioral effects to aquatic organisms chronically exposed to low levels of OWC mixtures are needed. ?? 2009 Elsevier B.V.

  20. SOURCES OF TOXIC COMPOUNDS IN HOUSEHOLD WASTEWATER

    EPA Science Inventory

    This report presents the results of a literature search into the occurrence of EPA's selected 129 priority pollutants in household wastewater. The study identifies consumer product categories and general types of products containing the toxic compounds used in and around the home...

  1. Widespread detection of N,N-diethyl-m-toluamide in U.S. streams: Comparison with concentrations of pesticides, personal care products, and other organic wastewater compounds

    USGS Publications Warehouse

    Sandstrom, M.W.; Kolpin, D.W.; Thurman, E.M.; Zaugg, S.D.

    2005-01-01

    One of the most frequently detected organic chemicals in a nationwide study concerning the effects of wastewater on stream water quality conducted in the year 2000 was the widely used insect repellant N,N-diethyl-m-toluamide (DEET). It was detected at levels of 0.02 ??g/L or greater in 73% of the stream sites sampled, with the selection of sampling sites being biased toward streams thought to be subject to wastewater contamination (i.e., downstream from intense urbanization and livestock production). Although DEET frequently was detected at all sites, the median concentration was low (0.05 ??g/L). The highest concentrations of DEET were found in streams from the urban areas (maximum concentration, 1.1 ??g/L). The results of the present study suggest that the movement of DEET to streams through wastewater-treatment systems is an important mechanism that might lead to the exposure of aquatic organisms to this chemical. ?? 2005 SETAC.

  2. Occurrence and fate of organic contaminants during onsite wastewater treatment

    USGS Publications Warehouse

    Conn, K.E.; Barber, L.B.; Brown, G.K.; Siegrist, R.L.

    2006-01-01

    Onsite wastewater treatment systems serve approximately 25% of the U.S. population. However, little is known regarding the occurrence and fate of organic wastewater contaminants (OWCs), including endocrine disrupting compounds, during onsite treatment. A range of OWCs including surfactant metabolites, steroids, stimulants, metal-chelating agents, disinfectants, antimicrobial agents, and pharmaceutical compounds was quantified in wastewater from 30 onsite treatment systems in Summit and Jefferson Counties, CO. The onsite systems represent a range of residential and nonresidential sources. Eighty eight percent of the 24 target compounds were detected in one or more samples, and several compounds were detected in every wastewater sampled. The wastewater matrices were complex and showed unique differences between source types due to differences in water and consumer product use. Nonresidential sources generally had more OWCs at higher concentrations than residential sources. Additional aerobic biofilter-based treatment beyond the traditional anaerobic tank-based treatment enhanced removal for many OWCs. Removal mechanisms included volatilization, biotransformation, and sorption with efficiencies from 99% depending on treatment type and physicochemical properties of the compound. Even with high removal rates during confined unit onsite treatment, OWCs are discharged to soil dispersal units at loadings up to 20 mg/m2/d, emphasizing the importance of understanding removal mechanisms and efficiencies in onsite treatment systems that discharge to the soil and water environments. ?? 2006 American Chemical Society.

  3. SORPTION OF ORGANICS ON WASTEWATER SOLIDS: CORRELATION WITH FUNDAMENTAL PROPERTIES.

    EPA Science Inventory

    Sorption of toxic organic compounds on primary, mixed-liquor, and digested solids from municipal wastewater treatment plants has been correlated with octanol/water partition coefficients arid with modified Randic indexes. he correlations developed are useful for assessing the rol...

  4. AEROBIC BIOTRANSFORMATION OF TOXIC ORGANICS IN WASTEWATER

    E-print Network

    #12;AEROBIC BIOTRANSFORMATION OF TOXIC ORGANICS IN WASTEWATER DOE FRAP 1997-15 Prepared for under three environments - anaerobic, anoxic- denitrifying and aerobic: Environment Variables Levels Studied Aerobic Dissolved Oxygen Conc. Cosubstrate Conc. 2 3 Anaerobic Anoxic Denitrifying Cosubstrate

  5. Evaluation of the treatment performance of lab-scaled vertical flow constructed wetlands in removal of organic compounds, color and nutrients in azo dye-containing wastewater.

    PubMed

    Dogdu, Gamze; Yalcuk, Arda

    2016-02-01

    The objective of this study is to examine the treatment performance of vertical flow intermittent feeding constructed wetland (VFCW) in removal of organic pollution, nutrients and color in azo-dye containing wastewater. The systems consisted of PVC reactors, some filling materials such as gravel, sand and zeolite and wetland plants including Typha angustifolia and Canna indica. The average treatment efficiency of the systems for COD, color, sulphate, NH4-N, and PO4-P were in the range of 57-63%, 94-99%, 44-48%, 39-44%, and 84-88%, respectively among the VFCW reactors. It is concluded that VFCW reactor system can effectively be used in the treatment of dye-rich wastewater, especially for the removal of color and in the reduction of COD. Biofilm formation and cleavage of azo bonds could be observed by SEM and FTIR results, respectively. Almost similar NH4-N and PO4-P removal were obtained in all reactors by using same amount of zeolite media. PMID:26248021

  6. SAMPLING FOR ORGANIC COMPOUNDS

    EPA Science Inventory

    The methods of sampling ambient air for organic compounds for subsequent analysis are discussed. The following methods of sample collection are presented and the advantages and disadvantages of each is given: concentration of component of interest on to solid sorbents, into liqui...

  7. EMISSIONS OF METALS, CHROMIUM AND NICKEL SPECIES, AND ORGANICS FROM MUNICIPAL WASTEWATER SLUDGE INCINERATORS

    EPA Science Inventory

    In order to provide data to support regulations on municipal wastewater sludge incineration, emissions of metals, hexavalent chromium, nickel subsulfide, polychlorinated dibenzo-dioxins and furans (PCDD/PCDFs), semivolatile and volatile organic compounds, carbon monoxide (CO)...

  8. Bioremediation of organic pollutants in a radioactive wastewater

    SciTech Connect

    Oboirien, Bilainu; Molokwane, P.E.; Chirwa, Evans

    2007-07-01

    Bioremediation holds the promise as a cost effective treatment technology for a wide variety of hazardous pollutants. In this study, the biodegradation of organic compounds discharged together with radioactive wastes is investigated. Nuclear process wastewater was simulated by a mixture of phenol and strontium, which is a major radionuclide found in radioactive wastewater. Phenol was used in the study as a model compound due to its simplicity of molecular structure. Moreover, the biodegradation pathway of phenol is well known. Biodegradation studies were conducted using pure cultures of Pseudomonas aeruginosa and Pseudomonas putida. The rate of phenol degradation by both species was found to be higher in the test without strontium. This suggests some degree of inhibition in the degradation of phenol by strontium. There was no phenol degradation in the sterile controls. The results indicate the feasibility of the biodegradation of organic pollutants discharged in radioactive effluents by specialised microbial cultures. (authors)

  9. Determination of potentially bioaccumulating complex mixtures of organochlorine compounds in wastewater: a review.

    PubMed

    Contreras López, M Concepción

    2003-03-01

    Organic chlorine compounds can be persistent environmental contaminants and may be accumulated through the food chain to the aquatic organisms, to fish and humans, depending basically on their hydrophobic properties. Consequently, there is an interest to measure these organic compounds from both the scientific and regulatory communities. The analytical essays have been improved for measuring specific organic chlorine compounds that present the most toxicological potential (polychlorinated biphenyls [PCBs], certain pesticides and dioxins), although they are tedious and time-consuming procedures. The existing tests to measure adsorbable organic halogens (AOX) or extractable organic halogens (EOX) do not distinguish the more hydrophobic organic chlorine matter. The intention of this paper is to make a review of the existing methods to measure the potentially bioaccumulating organochlorine compounds (OCs) from wastewater and propose a methodology to a standardisation procedure for complex mixtures of OCs in wastewater, such as pulp mill effluents. A new method has been proposed for determining the most hydrophobic part of the extractable organic halogens (EOX(fob)), the lowest reported value is 0.6 microg/l, expressed as chloride, and the relative standard deviation at 20 microg/l is 7% on laboratory samples and 30% on real effluents. This new procedure could be a valuable tool to complement environmental risk assessment studies of wastewater discharges. PMID:12605924

  10. Analysis and advanced oxidation treatment of a persistent pharmaceutical compound in wastewater and wastewater sludge-carbamazepine.

    PubMed

    Mohapatra, D P; Brar, S K; Tyagi, R D; Picard, P; Surampalli, R Y

    2014-02-01

    Pharmaceutically active compounds (PhACs) are considered as emerging environmental problem due to their continuous input and persistence to the aquatic ecosystem even at low concentrations. Among them, carbamazepine (CBZ) has been detected at the highest frequency, which ends up in aquatic systems via wastewater treatment plants (WWTPs) among other sources. The identification and quantification of CBZ in wastewater (WW) and wastewater sludge (WWS) is of major interest to assess the toxicity of treated effluent discharged into the environment. Furthermore, WWS has been subjected for re-use either in agricultural application or for the production of value-added products through the route of bioconversion. However, this field application is disputable due to the presence of these organic compounds and in order to protect the ecosystem or end users, data concerning the concentration, fate, behavior as well as the perspective of simultaneous degradation of these compounds is urgently necessary. Many treatment technologies, including advanced oxidation processes (AOPs) have been developed in order to degrade CBZ in WW and WWS. AOPs are technologies based on the intermediacy of hydroxyl and other radicals to oxidize recalcitrant, toxic and non-biodegradable compounds to various by-products and eventually to inert end products. The purpose of this review is to provide information on persistent pharmaceutical compound, carbamazepine, its ecological effects and removal during various AOPs of WW and WWS. This review also reports the different analytical methods available for quantification of CBZ in different contaminated media including WW and WWS. PMID:24140682

  11. Sorption behavior of potential organic wastewater indicators with soils.

    PubMed

    Yu, Liang; Fink, Guido; Wintgens, Thomas; Melin, Thomas; Ternes, Thomas A

    2009-03-01

    Soil-aquifer treatment is a wastewater treatment and reclamation option to facilitate beneficial water reuse. The fate of wastewater originated micropollutants in the soil-aquifer system is important to understand. In the study the sorption behavior of potential wastewater indicators such as two antiepileptic drugs (carbamazepine, primidone), one sulfonamide (sulfamethoxazole), and one corrosion inhibitor (benzotriazole) were determined with three natural soils (Lufa 2.2, Euro Soil 5, and Wulpen sand) that differed in pH, organic carbon content and particle size distribution. As aqueous phase a 0.01M CaCl(2) solution as well as the effluent of a municipal wastewater treatment plant was used. Affinities of all analytes to the soil increased from Wulpen sand, over Lufa 2.2 to Euro Soil 5, indicating that the organic carbon contents might be crucial for sorption. Isotherms were well described by the Freundlich model. Sorption was mainly close to linear (n=0.93-1.07) for most target compounds and soils. Desorption gave rise to a small hysteresis only for Euro Soil 5 which was likely artificial, due to slow desorption kinetics beyond 24h used in the experiment. All sorption studies confirmed that Carbamazepine, Benzotriazole and Primidone are appropriate to be used as wastewater indicator substances based on their low sorption affinity to soils, while the suitability of Sulfamethoxazole is limited due to the formation of non-extractable residues, especially at lower pH values. PMID:19095277

  12. Removal of cyanide compounds from coking wastewater by ferrous sulfate: Improvement of biodegradability.

    PubMed

    Yu, Xubiao; Xu, Ronghua; Wei, Chaohai; Wu, Haizhen

    2016-01-25

    The effect of ferrous sulfate (FeSO4) treatment on the removal of cyanide compounds and the improvement of biodegradability of coking wastewater were investigated by varying Fe:TCN molar ratios. Results suggested that the reaction between FeSO4 and coking wastewater was a two-step process. At the first step, i.e., 0?Fe:TCN?1.0, the reaction mechanisms were dominated by the precipitation of FeS, the complexation of CN(-), and the coagulation of organic compounds. The COD of coking wastewater decreased from 3748.1mg/L to 3450.2mg/L, but BOD5:COD (B/C) was improved from 0.30 to 0.51. At the second step, i.e., 1.0compounds by ferrous ions was the dominating mechanism. The COD showed a continuous increase to 3542.2mg/L (Fe:TCN=3.2) due to the accumulated ferrous ions in coking wastewater. Moreover, B/C decreased progressively to 0.35, which was attributed to the negative effects of excess ferrous ions on biodegradability. To improve coking wastewater's biodegradability, a minimum ferrous dosage is required to complete the first step reaction. However, the optimum ferrous dosage should be determined to control a safe residual TCN in coking wastewater for the further biological treatment. PMID:26547041

  13. Occurrence of Endocrine-Disrupting and Other Wastewater Compounds during Water Treatment with Case Studies from Lincoln, Nebraska and Berlin, Germany

    EPA Science Inventory

    Except for herbicides, research on the fate and transport of endocrine disrupting compounds and other organic wastewater compounds released into the environment and their potential presence in drinking water is in its infancy. Analytical methods still are being developed, evalua...

  14. Removal of phenolic compounds from wastewaters using soybean peroxidase

    SciTech Connect

    Wright, H.; Nicell, J.A.

    1996-11-01

    Toxic and odiferous phenolic compounds are present in wastewaters generated by a variety of industries including petroleum refining, plastics, resins, textiles, and iron and steel manufacturing among others. Due to its commercial availability in purified form, its useful presence in raw plant material, and its proven ability to remove a variety of phenolic contaminants from wastewaters over a wide range of pH and temperature, horseradish peroxidase (HRP) appears to be the peroxidase enzyme of choice in enzymatic wastewater treatment studies. Problems with HRP catalyzed phenol removal, however, include the formation of toxic soluble reaction by-products, the cost of the enzyme, and costs associated with disposal of the phenolic precipitate generated. Enzyme costs are incurred because the enzyme is inactivated during the phenol removal process by various side reactions. While recent work has shown that enzyme inactivation can be reduced using chemical additives, the problem of enzyme cost could be circumvented by using a less expensive source of enzyme. In 1991, the seed coat of the soybean was identified as a very rich source of peroxidase enzyme. Since the seed coat of the soybean is a waste product of the soybean food industry, soybean peroxidase (SBP) has the potential of being a cost effective alternative to HRP in wastewater treatment. In this study, SBP is characterized in terms of its catalytic activity, its stability, and its ability to promote removal of phenolic compounds from synthetic wastewaters. Results obtained are discussed and compared to similar investigations using HRP.

  15. Organic Compounds in Carbonaceous Meteorites

    NASA Technical Reports Server (NTRS)

    Cooper, Grorge

    2001-01-01

    Carbonaceous meteorites are relatively enriched in soluble organic compounds. To date, these compounds provide the only record available to study a range of organic chemical processes in the early Solar System chemistry. The Murchison meteorite is the best-characterized carbonaceous meteorite with respect to organic chemistry. The study of its organic compounds has related principally to aqueous meteorite parent body chemistry and compounds of potential importance for the origin of life. Among the classes of organic compounds found in Murchison are amino acids, amides, carboxylic acids, hydroxy acids, sulfonic acids, phosphonic acids, purines and pyrimidines (Table 1). Compounds such as these were quite likely delivered to the early Earth in asteroids and comets. Until now, polyhydroxylated compounds (polyols), including sugars (polyhydroxy aldehydes or ketones), sugar alcohols, sugar acids, etc., had not been identified in Murchison. Ribose and deoxyribose, five-carbon sugars, are central to the role of contemporary nucleic acids, DNA and RNA. Glycerol, a three-carbon sugar alcohol, is a constituent of all known biological membranes. Due to the relative lability of sugars, some researchers have questioned the lifetime of sugars under the presumed conditions on the early Earth and postulated other (more stable) compounds as constituents of the first replicating molecules. The identification of potential sources and/or formation mechanisms of pre-biotic polyols would add to the understanding of what organic compounds were available, and for what length of time, on the ancient Earth.

  16. Refractory organic pollutants and toxicity in pulp and paper mill wastewaters.

    PubMed

    Lindholm-Lehto, Petra C; Knuutinen, Juha S; Ahkola, Heidi S J; Herve, Sirpa H

    2015-05-01

    This review describes medium and high molecular weight organic material found in wastewaters from pulp and paper industry. The aim is to review the versatile pollutants and the analysis methods for their determination. Among other pollutants, biocides, extractives, and lignin-derived compounds are major contributors to harmful effects, such as toxicity, of industrial wastewaters. Toxicity of wastewaters from pulp and paper mills is briefly evaluated including the methods for toxicity analyses. Traditionally, wastewater purification includes mechanical treatment followed by chemical and/or biological treatment processes. A variety of methods are available for the purification of industrial wastewaters, including aerobic and anaerobic processes. However, some fractions of organic material, such as lignin and its derivatives, are difficult to degrade. Therefore, novel chemical methods, including electrochemical and oxidation processes, have been developed for separate use or in combination with biological treatment processes. PMID:25647495

  17. ENVIRONMENTAL BIOTECHNOLOGY Electricity generation from model organic wastewater

    E-print Network

    ENVIRONMENTAL BIOTECHNOLOGY Electricity generation from model organic wastewater in a cassette-008-1516-0 T. Shimoyama :S. Komukai :K. Watanabe Laboratory of Applied Microbiology, Marine Biotechnology

  18. PERSISTENT PERFLUORINATED ORGANIC COMPOUNDS

    EPA Science Inventory

    Perfluorinated compounds (PFCs) have gained notoriety in the recent past. Global distribution of PFCs in wildlife, environmental samples and humans has sparked a recent increase in new investigations concerning PFCs. Historically PFCs have been used in a wide variety of consume...

  19. Antibiotic, Pharmaceutical, and Wastewater-Compound Data for Michigan, 1998-2005

    USGS Publications Warehouse

    Haack, Sheridan Kidd

    2010-01-01

    Beginning in the late 1990's, the U.S. Geological Survey began to develop analytical methods to detect, at concentrations less than 1 microgram per liter (ug/L), emerging water contaminants such as pharmaceuticals, personal-care chemicals, and a variety of other chemicals associated with various human and animal sources. During 1998-2005, the U.S. Geological Survey analyzed the following Michigan water samples: 41 samples for antibiotic compounds, 28 samples for pharmaceutical compounds, 46 unfiltered samples for wastewater compounds (dissolved and suspended compounds), and 113 filtered samples for wastewater compounds (dissolved constituents only). The purpose of this report is to summarize the status of emerging contaminants in Michigan waters based on data from several different project-specific sample-collection efforts in Michigan during an 8-year period. During the course of the 8-year sampling effort, antibiotics were determined at 20 surface-water sites and 2 groundwater sites, pharmaceuticals were determined at 11 surface-water sites, wastewater compounds in unfiltered water were determined at 31 surface-water sites, and wastewater compounds in filtered water were determined at 40 surface-water and 4 groundwater sites. Some sites were visited only once, but others were visited multiple times. A variety of quality-assurance samples also were collected. This report describes the analytical methods used, describes the variations in analytical methods and reporting levels during the 8-year period, and summarizes all data using current (2009) reporting criteria. Very few chemicals were detected at concentrations greater than current laboratory reporting levels, which currently vary from a low of 0.005 ug/L for some antibiotics to 5 ug/L for some wastewater compounds. Nevertheless, 10 of 51 chemicals in the antibiotics analysis, 9 of 14 chemicals in the pharmaceuticals analysis, 34 of 67 chemicals in the unfiltered-wastewater analysis, and 56 of 62 chemicals in the filtered-wastewater analysis were detected. Antibiotics were detected at 7 of 20 tested surface-water sites, but none were detected in 2 groundwater samples. Pharmaceuticals were detected at 7 of 11 surface-water sites. Wastewater compounds were detected at 25 of 31 sites for which unfiltered water samples were analyzed and at least once at all 40 surface-water sites and all 4 groundwater sites for which filtered water samples were analyzed. Overall, the chemicals detected most frequently in Michigan waters were similar to those reported frequently in other studies nationwide. Patterns of chemical detections were site specific and appear to be related to local sources, overall land use, and hydrologic conditions at the time of sampling. Field-blank results provide important information for the design of future sampling programs in Michigan and demonstrate the need for careful field-study design. Field-replicate results indicated substantial confidence regarding the presence or absence of the many chemicals tested. Overall, data reported herein indicate that a wide array of antibiotic, pharmaceutical, and organic wastewater compounds occur in Michigan waters. Patterns of occurrence, with respect to hydrologic, land use, and source variables, generally appear to be similar for Michigan as for other sampled waters across the United States. The data reported herein can serve as a basis for future studies in Michigan.

  20. Organic Compounds in Stardust

    NASA Technical Reports Server (NTRS)

    McKay, David S.; Clemett. Simon J.; Sandford, Scott A.; Nakamura-Messenger, Keiko; Hoerz, Fredrich

    2011-01-01

    The successful return of the STARDUST spacecraft provides a unique opportunity to investigate the nature and distribution of organic matter in cometary dust particles collected from Comet 81P/Wild-2. Analysis of individual cometary impact tracks in silica aerogel using the technique of two-step laser mass spectrometry (L2MS) demonstrates the presence of complex aromatic organic matter. While concerns remain as to the organic purity of the aerogel collection medium and the thermal effects associated with hypervelocity capture, the majority of the observed organic species appear indigenous to the impacting particles and are hence of cometary origin. While the aromatic fraction of the total organic matter present is believed to be small, it is notable in that it appears to be N-rich. Spectral analysis in combination with instrumental detection sensitivities suggest that N is incorporated predominantly in the form of aromatic nitriles (R-C N). While organic species in the STARDUST samples do share some similarities with those present in the matrices of carbonaceous chondrites, the closest match is found with stratospherically collected interplanetary dust particles. These findings are consistent with the notion that a fraction of interplanetary dust is of cometary origin. The presence of complex organic N-containing species in comets has astrobiological implications since comets are likely to have contributed to the prebiotic chemical inventory of both the Earth and Mars.

  1. Biomedical Compounds from Marine organisms

    PubMed Central

    Jha, Rajeev Kumar; Zi-rong, Xu

    2004-01-01

    The Ocean, which is called the ‘mother of origin of life’, is also the source of structurally unique natural products that are mainly accumulated in living organisms. Several of these compounds show pharmacological activities and are helpful for the invention and discovery of bioactive compounds, primarily for deadly diseases like cancer, acquired immuno-deficiency syndrome (AIDS), arthritis, etc., while other compounds have been developed as analgesics or to treat inflammation, etc. The life-saving drugs are mainly found abundantly in microorganisms, algae and invertebrates, while they are scarce in vertebrates. Modern technologies have opened vast areas of research for the extraction of biomedical compounds from oceans and seas.

  2. Extraterrestrial Organic Compounds in Meteorites

    NASA Technical Reports Server (NTRS)

    Botta, Oliver; Bada, Jeffrey L.; Meyer, Michael (Technical Monitor)

    2003-01-01

    Many organic compounds or their precursors found in meteorites originated in the interstellar or circumstellar medium and were later incorporated into planetesimals during the formation of the solar system. There they either survived intact or underwent further processing to synthesize secondary products on the meteorite parent body. The most distinct feature of CI and CM carbonaceous chondrites, two types of stony meteorites, is their high carbon content (up to 3% of weight), either in the form of carbonates or of organic compounds. The bulk of the organic carbon consists of an insoluble macromolecular material with a complex structure. Also present is a soluble organic fraction, which has been analyzed by several separation and analytical procedures. Low detection limits can be achieved by derivatization of the organic molecules with reagents that allow for analysis by gas chromatography/mass spectroscopy and high performance liquid chromatography. The CM meteorite Murchison has been found to contain more than 70 extraterrestrial amino acids and several other classes of compounds including carboxylic acids, hydroxy carboxylic acids, sulphonic and phosphonic acids, aliphatic, aromatic and polar hydrocarbons, fullerenes, heterocycles as well as carbonyl compounds, alcohols, amines and amides. The organic matter was found to be enriched in deuterium, and distinct organic compounds show isotopic enrichments of carbon and nitrogen relative to terrestrial matter.

  3. OPTIMIZATION OF MULTICOMPONENT PERVAPORATION FOR REMOVAL OF VOLATILE ORGANIC COMPOUNDS FROM WATER

    EPA Science Inventory

    Optimal operation of a hollow fiber membrane module for pervaporative removal of multicomponent volatile organic compounds (VOCs) from wastewater was studied. A shell-and-tube heat-exchange type of hollow fiber module was considered for treatment of a wastewater containing toluen...

  4. OPTIMIZATION OF MULTICOMPONENT PERVAPORATION FOR REMOVAL OF VOLATILE ORGANIC COMPOUNDS FROM WATER

    EPA Science Inventory

    Optimal operation of a hollow fiber membrane module for pervaporative removal of multicomponent volatile organic compounds (VOCS) from wastewater was studied. hell-and-tube heat-exchanger type of hollow fiber module was considered for treatment of a wastewater containing toluene,...

  5. Role of fly ash in the removal of organic pollutants from wastewater

    SciTech Connect

    M. Ahmaruzzaman

    2009-03-15

    Fly ash, a relatively abundant and inexpensive material, is currently being investigated as an adsorbent for the removal of various organic pollutants from wastewater. The wastewater contains various types of phenolic compounds, such as chloro, nitro, amino, and other substituted compounds. Various types of pesticides, such as lindane, malathion, carbofuran, etc., and dyes, such as, methylene blue, crystal violet, malachite green, etc., are also present in the wastewater. These contaminants pollute the water stream. These organic pollutants, such as phenolic compounds, pesticides, and dyes, etc., can be removed very effectively using fly ash as adsorbent. This article presents a detailed review on the role of fly ash in the removal of organic pollutants from wastewater. Adsorption of various pollutants using fly ash has been reviewed. The adsorption mechanism and other influencing factors, favorable conditions, and competitive ions, etc., on the adsorption process have also been discussed in this paper. It is evident from the review that fly ash has demonstrated good removal capabilities for various organic compounds. 171 refs., 3 figs., 5 tabs.

  6. Synergistic Antibacterial Effects of Polyphenolic Compounds from Olive Mill Wastewater

    PubMed Central

    Tafesh, Ahmed; Najami, Naim; Jadoun, Jeries; Halahlih, Fares; Riepl, Herbert; Azaizeh, Hassan

    2011-01-01

    Polyphenols or phenolic compounds are groups of secondary metabolites widely distributed in plants and found in olive mill wastewater (OMW). Phenolic compounds as well as OMW extracts were evaluated in vitro for their antimicrobial activity against Gram-positive (Streptococcus pyogenes and Staphylococcus aureus) and Gram-negative bacteria (Escherichia coli and Klebsiella pneumoniae). Most of the tested phenols were not effective against the four bacterial strains when tested as single compounds at concentrations of up to 1000??g?mL?1. Hydroxytyrosol at 400??g?mL?1 caused complete growth inhibition of the four strains. Gallic acid was effective at 200, and 400??g?mL?1 against S. aureus, and S. pyogenes, respectively, but not against the gram negative bacteria. An OMW fraction called AntiSolvent was obtained after the addition of ethanol to the crude OMW. HPLC analysis of AntiSolvent fraction revealed that this fraction contains mainly hydroxytyrosol (10.3%), verbascoside (7.4%), and tyrosol (2.6%). The combinations of AntiSolvent/gallic acid were tested using the low minimal inhibitory concentrations which revealed that 50/100–100/100??g?mL?1 caused complete growth inhibition of the four strains. These results suggest that OMW specific fractions augmented with natural phenolic ingredients may be utilized as a source of bioactive compounds to control pathogenic bacteria. PMID:21647315

  7. In vivo endocrine disruption assessment of wastewater treatment plant effluents with small organisms.

    PubMed

    Castillo, Luis; Seriki, Kemi; Mateos, Stéphanie; Loire, Nicolas; Guédon, Nathalie; Lemkine, Gregory F; Demeneix, Barbara A; Tindall, Andrew J

    2013-01-01

    Surface water receives a variety of micro-pollutants that could alter aquatic organisms' reproduction and development. It is known that a few nanograms per litre of these compounds can induce endocrine-disrupting effects in aquatic species. Many compounds are released daily in wastewater, and identifying the compounds responsible for inducing such disruption is difficult. Methods using biological analysis are therefore an alternative to chemical analysis, as the endocrine disruption potential of the stream as a whole is considered. To detect hormonal disruption of thyroid and oestrogenic functions, fluorescent Xenopus laevis tadpoles and medaka (Oryzias latipes) fish larvae bearing genetic constructs integrating hormonal responsive elements were used for physiological screens for potential endocrine disruption in streams from an urban wastewater treatment plant. The Xenopus model was used to assess thyroid disruption and the medaka model oestrogenic disruption in wastewater samples. Assays using the genetically modified organisms were conducted on 9 influent and 32 effluent samples. The thyroidal effect of wastewater was either reduced or removed by the treatment plant; no oestrogenic effect was detected in any of the wastewater samples. PMID:23823564

  8. Volatile Organic Compounds in Uremia

    PubMed Central

    Seifert, Luzia; Slodzinski, Rafael; Jankowski, Joachim; Zidek, Walter; Westhoff, Timm H.

    2012-01-01

    Background Although “uremic fetor” has long been felt to be diagnostic of renal failure, the compounds exhaled in uremia remain largely unknown so far. The present work investigates whether breath analysis by ion mobility spectrometry can be used for the identification of volatile organic compounds retained in uremia. Methods Breath analysis was performed in 28 adults with an eGFR ?60 ml/min per 1.73 m2, 26 adults with chronic renal failure corresponding to an eGFR of 10–59 ml/min per 1.73 m2, and 28 adults with end-stage renal disease (ESRD) before and after a hemodialysis session. Breath analysis was performed by ion mobility spectrometryafter gas-chromatographic preseparation. Identification of the compounds of interest was performed by thermal desorption gas chromatography/mass spectrometry. Results Breath analyses revealed significant differences in the spectra of patients with and without renal failure. Thirteen compounds were chosen for further evaluation. Some compounds including hydroxyacetone, 3-hydroxy-2-butanone and ammonia accumulated with decreasing renal function and were eliminated by dialysis. The concentrations of these compounds allowed a significant differentiation between healthy, chronic renal failure with an eGFR of 10–59 ml/min, and ESRD (p<0.05 each). Other compounds including 4-heptanal, 4-heptanone, and 2-heptanone preferentially or exclusively occurred in patients undergoing hemodialysis. Conclusion Impairment of renal function induces a characteristic fingerprint of volatile compounds in the breath. The technique of ion mobility spectrometry can be used for the identification of lipophilic uremic retention molecules. PMID:23049998

  9. Fate of trace organics in a wastewater effluent dependent stream.

    PubMed

    Dong, Bingfeng; Kahl, Alandra; Cheng, Long; Vo, Hao; Ruehl, Stephanie; Zhang, Tianqi; Snyder, Shane; Sáez, A Eduardo; Quanrud, David; Arnold, Robert G

    2015-06-15

    Trace organic compounds (TOrCs) in municipal wastewater effluents that are discharged to streams are of potential concern to ecosystem and human health. This study examined the fate of a suite of TOrCs and estrogenic activity in water and sediments in an effluent-dependent stream in Tucson, Arizona. Sampling campaigns were performed during 2011 to 2013 along the Lower Santa Cruz River, where TOrCs and estrogenic activity were measured in aqueous (surface) and solid (riverbed sediment) phases. Some TOrCs, including contributors to estrogenic activity, were rapidly attenuated with distance of travel in the river. Those TOrCs that are not sufficiently attenuated and percolate to ground water have in common low biodegradation probabilities and low octanol-water distribution ratios. Independent experiments showed that attenuation of estrogenic compounds may be due in part to indirect photolysis caused by formation of organic radicals from sunlight absorption. Hydrophobic TOrCs may accumulate in riverbed sediments during dry weather periods, but riverbed sediment quality is periodically affected through storm-related scouring during periods of heavy rainfall and runoff. Taken together, evidence suggests that natural processes can attenuate at least some TOrCs, reducing potential impacts to ecosystem and human health. PMID:25777953

  10. Chapter A5. Section 6.1.F. Wastewater, Pharmaceutical, and Antibiotic Compounds

    USGS Publications Warehouse

    Lewis, Michael Edward; Zaugg, Steven D.

    2003-01-01

    The USGS differentiates between samples collected for analysis of wastewater compounds and those collected for analysis of pharmaceutical and antibiotic compounds, based on the analytical schedule for the laboratory method. Currently, only the wastewater laboratory method for field-filtered samples (SH1433) is an approved, routine (production) method. (The unfiltered wastewater method LC 8033 also is available but requires a proposal for custom analysis.) At this time, analysis of samples for pharmaceutical and antibiotic compounds is confined to research studies and is available only on a custom basis.

  11. Potential endocrine disrupting organic chemicals in treated municipal wastewater and river water

    USGS Publications Warehouse

    Barber, L.B.; Brown, G.K.; Zaugg, S.D.

    2000-01-01

    Select endocrine disrupting organic chemicals were measured in treated wastewater from Chicago, IL, Minneapolis/St. Paul, MN, Detroit, MI, and Milwaukee, WI, and in the Des Plaines, Illinois, and Minnesota Rivers during the fall of 1997 and the spring of 1998. Emphasis was given to alkylphenolpolyethoxylate (APEO) derived compounds, although 17-??-estradiol, bisphenol A, caffeine, total organic carbon, ethylenediaminetetraacetic acid (EDTA), and other compounds also were measured. Contaminants were isolated by continuous liquid-liquid extraction (CLLE) with methylene chloride and analyzed by gas chromatography/mass spectrometry in full scan and selected ion monitoring modes. The extracts were derivatized to form the methyl esters of alkylphenolethoxycarboxylates (APEC), and EDTA was isolated by evaporation and derivatized to form the tetrapropyl ester. The mass spectra of nonylphenol (NP) and octylphenol (OP) compounds are complex and show variations among the different ethoxylate and carboxylate homologs, reflecting variations in the ethylene oxide chain length. Recoveries for target compounds and surrogate standards ranged from 20-130%, with relative standard deviations of 9.9-53%. Detection limits for the various compounds ranged from 0.06-0.35 ??g/L. Analysis of the wastewater effluents detected a number of compounds including NP, NPEO, OP, OPEO, NPEC, caffeine, and EDTA at concentrations ranging from <1-439 ??g/L, with EDTA and NPEC being most abundant. There was variability in compound distributions and concentrations between the various sewage treatment plants, indicating differences in treatment type and influent composition. Several wastewater-derived compounds were detected in the river samples, with EDTA and NPEC persisting for considerable distance downstream from wastewater discharges, and NP and NPEO being attenuated more rapidly.

  12. 40 CFR Table 34 to Subpart G of... - Fraction Measured (Fm) and Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams 34 Table 34 to Subpart G...Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 34 Table...Emitted (Fe ) For HAP Compounds in Wastewater Streams Chemical name CAS...

  13. 40 CFR Table 34 to Subpart G of... - Fraction Measured (Fm) and Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams 34 Table 34 to Subpart G...Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 34 Table...Emitted (Fe ) For HAP Compounds in Wastewater Streams Chemical name CAS...

  14. 40 CFR Table 34 to Subpart G of... - Fraction Measured (Fm) and Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams 34 Table 34 to Subpart G...Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 34 Table...Emitted (Fe ) For HAP Compounds in Wastewater Streams Chemical name CAS...

  15. 40 CFR Table 34 to Subpart G of... - Fraction Measured (Fm) and Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams 34 Table 34 to Subpart G...Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 34 Table...Emitted (Fe ) For HAP Compounds in Wastewater Streams Chemical name CAS...

  16. Volatile organic compound sensor system

    DOEpatents

    Schabron, John F. (Laramie, WY); Rovani, Jr., Joseph F. (Laramie, WY); Bomstad, Theresa M. (Laramie, WY); Sorini-Wong, Susan S. (Laramie, WY)

    2009-02-10

    Generally, this invention relates to the development of field monitoring methodology for new substances and sensing chemical warfare agents (CWAs) and terrorist substances. It also relates to a portable test kit which may be utilized to measure concentrations of halogenated volatile organic compounds (VOCs) in the field. Specifically it relates to systems for reliably field sensing the potential presence of such items while also distinguishing them from other elements potentially present. It also relates to overall systems and processes for sensing, reacting, and responding to an indicated presence of such substance, including modifications of existing halogenated sensors and arrayed sensing systems and methods.

  17. Volatile organic compound sensor system

    DOEpatents

    Schabron, John F. (Laramie, WY); Rovani, Jr., Joseph F. (Laramie, WY); Bomstad, Theresa M. (Waxahachie, TX); Sorini-Wong, Susan S. (Laramie, WY); Wong, Gregory K. (Laramie, WY)

    2011-03-01

    Generally, this invention relates to the development of field monitoring methodology for new substances and sensing chemical warfare agents (CWAs) and terrorist substances. It also relates to a portable test kit which may be utilized to measure concentrations of halogenated volatile organic compounds (VOCs) in the field. Specifically it relates to systems for reliably field sensing the potential presence of such items while also distinguishing them from other elements potentially present. It also relates to overall systems and processes for sensing, reacting, and responding to an indicated presence of such substance, including modifications of existing halogenated sensors and arrayed sensing systems and methods.

  18. Studies on electrochemical treatment of wastewater contaminated with organotin compounds.

    PubMed

    Arevalo, Eduardo; Calmano, Wolfgang

    2007-07-31

    Different anode materials were tested to evaluate their suitability to eliminate organotin compounds electrochemically from shipyard process waters. The capacity of two types of anode materials was investigated: niobium coated with boron-doped diamond (BDD) and titanium coated with iridium dioxide, (Ti/IrO(2)). The aim of this work was to characterize the performance of the process using both anode materials at different current densities, and also to evaluate the generation of by-products. A further objective of this work was to evaluate if operating at low potentials with BDD anodes (to avoid the generation of elemental oxygen) the consumption of energy for degradation of pollutants could be minimized. The processes were tested on synthetic and real shipyard water containing approximately 25,000ngL(-1) of tributyltin (TBT) (as Sn) and 5,000ngL(-1) dibutyltin. The range of current densities was between 6 and 70mAcm(-2). The results showed that electrochemical treatment is suitable to eliminate organotins down to very low concentrations following a stepwise debutylation mechanism. Both anode materials exhibited a similar performance with energy consumption in the range of 7-10kWhm(-3) in order to decrease organotins down to 100ngL(-1) (as Sn). For the water composition tested, BDD did not outperform Ti/IrO(2) as initially expected, most probably because organotins were not only oxidized by OH, but also by active chlorine compounds generated by the oxidation of chloride present in the wastewater (1.6gL(-1), Cl(-)) with both anode materials. It was also found that the residual oxidants remaining in the treated effluent had to be eliminated if the water is to be discharged safely in the aquatic environment. PMID:17521806

  19. Green Technology for the Removal of Chloro-Organics from Pulp and Paper Mill Wastewater.

    PubMed

    Choudhary, Ashutosh Kumar; Kumar, Satish; Sharma, Chhaya; Kumar, Vivek

    2015-07-01

    This study evaluates the treatment efficiency of a horizontal subsurface-flow constructed wetland (HSSF-CW) for the removal of chloro-organic compounds from pulp and paper mill wastewater. The surface area of the HSSF-CW unit was 5.25 m˛ and was planted with Colocasia esculenta. The wastewater was characterized for different chloro-organic compounds, that is, adsorbable organic halides (AOX), chlorophenolics, and chlorinated resin and fatty acids (cRFAs). Under a hydraulic retention time of 5.9 days, the average AOX, chlorophenolics, and cRFA removal from wastewater was 87, 87, and 93%, respectively. Some of the chlorophenolics were found to accumulate in the plant biomass and soil material. The mass balance studies show that a significant fraction of chlorophenolics and cRFA was degraded in the constructed wetland system. Modeling studies were carried out to estimate the first-order area-based removal rate constants (k) for chemical oxygen demand removal. The HSSF-CW was found to be an effective treatment technology for the remediation of pulp and paper mill wastewater. PMID:26163503

  20. DETERMINATION OF VOLATILE ORGANICS IN INDUSTRIAL AND MUNICIPAL WASTEWATERS

    EPA Science Inventory

    This report describes the systematic evaluation of a series of parameters leading to the development of a test procedure for 36 volatile priority pollutants in wastewaters. A study of the effect of pH, temperature, and residual chlorine on the aqueous stability of the compounds l...

  1. Electroreduction of Halogenated Organic Compounds

    NASA Astrophysics Data System (ADS)

    Rondinini, Sandra; Vertova, Alberto

    The electroreductive cleavage of the carbon-halogen bond in halogenated organic compounds has been extensively studied for more than 70 years, since it is prodromal to a large variety of synthetic applications in organic electrochemistry. Over the years the research interest have progressively included the environmental applications, since several organic halocompounds are known to have (or have had) a serious environmental impact because of their (present or past) wide use as cleaning agents, herbicides, cryogenic fluids, reagents (e.g. allyl and vinyl monomers) for large production materials, etc. Recent studies have also demonstrated the wide spread out- and in-door-presence of volatile organic halides, although at low level, in connexion with residential and non-residential (e.g. stores, restaurants and transportation) activities. In this context, the detoxification of emissions to air, water and land by the selective removal of the halogen group represents a valid treatment route, which, although not leading to the complete mineralization of the pollutants, produces less harmful streams to be easily treated by electrochemical or conventional techniques. The electroreduction process is analysed and discussed in terms of electrode material, reaction medium, cell design and operation, and of substrate classification.

  2. Soluble, semivolatile phenol and nitrogen compounds in milk-processing wastewaters.

    PubMed

    Verheyen, V; Cruickshank, A; Wild, K; Heaven, M W; McGee, R; Watkins, M; Nash, D

    2009-07-01

    Potable water is an essential and major input in processing our food supplies, and the continued growth in food manufacturing is placing increased pressure on this limited resource. Recycling and reuse of factory wastewater can lessen potable water use but requires a detailed understanding of wastewater properties. This study uses solid-phase extraction techniques with gas chromatography-mass spectrometry analysis to investigate trace-level semivolatile organic species in various waste and reference waters associated with the Burra Foods milk-processing plant located in Southeastern Australia. Our focus was on contaminants containing phenolic and heterocyclic nitrogen functional groups, which, because of their toxicity and persistence, may limit options for water recycling and reuse. Effluent from the wastewater treatment plant of the factory showed both the highest soluble carbon burden (47 mg/kg) and concentrations of target compounds. The target species found in these effluents included methyl phenol (13 mg/kg), hydroxy indole (9.8 mg/kg), synthetic tolyltriazoles (5.1 mg/kg) and alkyl phenol ethoxylates (0.2 mg/kg). Given the environmental stability of the tolyltriazoles, they may act as chemical markers where these effluents are used for purposes such as irrigation. Milk evaporator condensate waters, in contrast to the effluent, contained very few target species, with only low levels of pyrrolidine and piperidine derivatives such as ethylglutarimide (450 mug/L) detected. Although there were fewer target microcontaminants overall in the potable and creek reference waters, these samples had characteristic profiles. The potable water analysis revealed hydroxy cineole (2.1 microg/L) and the creek analysis revealed dichlorohydroxyacetophenone (0.3 microg/L), which were not detected in other waters. The compounds found in the wastewaters are likely to have been derived from milk or synthetic chemicals used in factory operations. The presence of nitrogen compounds in all the different milk-processing waters suggest their likely source was milk, probably milk phosphoproteins subjected to thermal, chemical, or microbial degradation. Our benign results for the condensates suggest it may be possible to substitute condensate for potable water with minimal pretreatment, both within the plant and in other applications, such as irrigation of recreation turf. PMID:19528627

  3. The ability of biologically based wastewater treatment systems to remove emerging organic contaminants--a review.

    PubMed

    Garcia-Rodríguez, Aida; Matamoros, Víctor; Fontŕs, Clŕudia; Salvadó, Victňria

    2014-10-01

    Biologically based wastewater treatment systems are considered a sustainable, cost-effective alternative to conventional wastewater treatment systems. These systems have been used and studied for the treatment of urban sewage from small communities, and recently, it has been reported that they can also effectively remove emerging organic contaminants (EOCs). EOCs are a new group of unregulated contaminants which include pharmaceutical and personal care products, some pesticides, veterinary products, and industrial compounds among others that are thought to have long-term adverse effects on human health and ecosystems. This review is focused on reporting the ability of biologically based wastewater treatment systems to remove EOCs and the main elimination mechanisms and degradation processes (i.e., biodegradation, photodegradation, phytoremediation, and sorption) taking place in constructed wetlands, ponds, and Daphnia and fungal reactors. PMID:24414147

  4. Removal of organic wastewater contaminants in septic systems using advanced treatment technologies

    USGS Publications Warehouse

    Wilcox, J.D.; Bahr, J.M.; Hedman, C.J.; Hemming, J.D.C.; Barman, M.A.E.; Bradbury, K.R.

    2009-01-01

    The detection of pharmaceuticals and other organic wastewater contaminants (OWCs) in ground water and surface-water bodies has raised concerns about the possible ecological impacts of these compounds on nontarget organisms. On-site wastewater treatment systems represent a potentially significant route of entry for organic contaminants to the environment. In this study, effluent samples were collected and analyzed from conventional septic systems and from systems using advanced treatment technologies. Six of 13 target compounds were detected in effluent from at least one septic system. Caffeine, paraxanthine, and acetaminophen were the most frequently detected compounds, and estrogenic activity was detected in 14 of 15 systems. The OWC concentrations were significantly lower in effluent after sand filtration (p < 0.01) or aerobic treatment (p < 0.05) as compared with effluent that had not undergone advanced treatment. In general, concentrations in conventional systems were comparable to those measured in previous studies of municipal wastewater treatment plant (WWTP) influent, and concentrations in systems after advanced treatment were comparable to previously measured concentrations in WWTP effluent. These data indicate that septic systems using advanced treatment can reduce OWCs in treated effluent to similar concentrations as municipal WWTPs. Copyright ?? 2009 by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America. All rights reserved.

  5. Volatile organic compound sensing devices

    DOEpatents

    Lancaster, Gregory D. (Idaho Falls, ID); Moore, Glenn A. (Idaho Falls, ID); Stone, Mark L. (Idaho Falls, ID); Reagen, William K. (Stillwater, MN)

    1995-01-01

    Apparatus employing vapochromic materials in the form of inorganic double complex salts which change color reversibly when exposed to volatile organic compound (VOC) vapors is adapted for VOC vapor detection, VOC aqueous matrix detection, and selective VOC vapor detection. The basic VOC vapochromic sensor is incorporated in various devices such as a ground probe sensor, a wristband sensor, a periodic sampling monitor, a soil/water penetrometer, an evaporative purge sensor, and various vacuum-based sensors which are particularly adapted for reversible/reusable detection, remote detection, continuous monitoring, or rapid screening of environmental remediation and waste management sites. The vapochromic sensor is used in combination with various fiber optic arrangements to provide a calibrated qualitative and/or quantitative indication of the presence of VOCs.

  6. Volatile organic compound sensing devices

    DOEpatents

    Lancaster, G.D.; Moore, G.A.; Stone, M.L.; Reagen, W.K.

    1995-08-29

    Apparatus employing vapochromic materials in the form of inorganic double complex salts which change color reversibly when exposed to volatile organic compound (VOC) vapors is adapted for VOC vapor detection, VOC aqueous matrix detection, and selective VOC vapor detection. The basic VOC vapochromic sensor is incorporated in various devices such as a ground probe sensor, a wristband sensor, a periodic sampling monitor, a soil/water penetrometer, an evaporative purge sensor, and various vacuum-based sensors which are particularly adapted for reversible/reusable detection, remote detection, continuous monitoring, or rapid screening of environmental remediation and waste management sites. The vapochromic sensor is used in combination with various fiber optic arrangements to provide a calibrated qualitative and/or quantitative indication of the presence of VOCs. 15 figs.

  7. REMOVAL OF PHENOLIC COMPOUNDS FROM WOOD PRESERVING WASTEWATERS

    EPA Science Inventory

    Laboratory and pilot-scale studies were undertaken to develop economically feasible technologies for the treatment of wastewaters from wood preserving operations. Of prime concern was the removal of phenol and its chlorinated derivatives, in particular, pentachlorophenol. Screeni...

  8. [FTIR and 13C NMR Analysis of Dissolved Organic Matter (DOM) in the Treatment Process of Tannery Wastewater].

    PubMed

    Fan, Chun-hui; Zhang, Ying-chao; Tang, Ze-heng; Wang, Jia-hong

    2015-05-01

    Nowadays, the wastewater quantity discharged yearly from tannery industry is around 0. 2 billion t in China. The contaminants of tannery wastewater include macromolecular organic matters, such as grease, fur scraps and collagen, and the alkaline wastewater appears to be of high content of salt and COD. The quality of tannery wastewater is monitored strictly among all kinds of industry wastewater. In the treatment process of tannery wastewater, the quality of inlet and outlet water is generally analyzed. In fact, the transformation behavior of contaminants should be additionally checked to optimize the treatment conditions. Dissolved organic matter (DOM) is commonly existed in water-bodies and helpful to understand the physicochemical characteristics, while the related work should be further studied on tannery wastewater. The approaches of elemental analysis, thermal gravimetric analysis (TG), Fourier infrared spectroscopy (FTIR) and 13C nuclear magnetic resonance (13C NMR) were used to reveal the characteristics of DOM in the treatment process of tannery wastewater. The results showed the carbon content of DOM samples increased gradually, atomic ratios of H/C increased firstly and then decreased, indicating the organic matters were decomposed into chain structures firstly, finally forming the component hard to degraded. The pyrolysis process of DOM mainly proceeded in the regions of 110~530 °C (aliphatic compound, protein, etc. ) and 530~800 °C (aromatic ring, single bond of C-C, etc. ). The functional groups of DOM included -OH, -NH2, C=O and so on, and the aromatic substances were detected, shown from FTIR figures, in the later period of the reaction, caused by the metabolism effect of micro-organism. The content of alkoxy-C increased to the maximum in the second biochemical pond, and the minimum content of aromatic-C appeared in the second biochemical pond, suggesting the transformation behavior of carbon functional groups. The investigation on DOM in tannery wastewater is significant to understand the purification mechanism of contaminants in tannery wastewater. PMID:26415428

  9. Winery waste makes fuel Electricity, bacteria break organics in wastewater into hydrogen gas

    E-print Network

    MSNBC.com Winery waste makes fuel Electricity, bacteria break organics in wastewater into hydrogen method for generating hydrogen fuel from wastewater is now operating at a California winery material in the wastewater into hydrogen gas. There is a lot more energy locked in the wastewater than

  10. Catalytic ozonation-biological coupled processes for the treatment of industrial wastewater containing refractory chlorinated nitroaromatic compounds*

    PubMed Central

    Li, Bing-zhi; Xu, Xiang-yang; Zhu, Liang

    2010-01-01

    A treatability study of industrial wastewater containing chlorinated nitroaromatic compounds (CNACs) by a catalytic ozonation process (COP) with a modified Mn/Co ceramic catalyst and an aerobic sequencing batch reactor (SBR) was investigated. A preliminary attempt to treat the diluted wastewater with a single SBR resulted in ineffective removal of the color, ammonia, total organic carbon (TOC) and chemical oxygen demand (COD). Next, COP was applied as a pretreatment in order to obtain a bio-compatible wastewater for SBR treatment in a second step. The effectiveness of the COP pretreatment was assessed by evaluating wastewater biodegradability enhancement (the ratio of biology oxygen demand after 5 d (BOD5) to COD), as well as monitoring the evolution of TOC, carbon oxidation state (COS), average oxidation state (AOS), color, and major pollutant concentrations with reaction time. In the COP, the catalyst preserved its catalytic properties even after 70 reuse cycles, exhibiting good durability and stability. The performance of SBR to treat COP effluent was also examined. At an organic loading rate of 2.0 kg COD/(m3·d), with hydraulic retention time (HRT)=10 h and temperature (30±2) °C, the average removal efficiencies of NH3-N, COD, BOD5, TOC, and color in a coupled COP/SBR process were about 80%, 95.8%, 93.8%, 97.6% and 99.3%, respectively, with average effluent concentrations of 10 mg/L, 128 mg/L, 27.5 mg/L, 25.0 mg/L, and 20 multiples, respectively, which were all consistent with the national standards for secondary discharge of industrial wastewater into a public sewerage system (GB 8978-1996). The results indicated that the coupling of COP with a biological process was proved to be a technically and economically effective method for treating industrial wastewater containing recalcitrant CNACs. PMID:20205304

  11. Fate of organic bases during biooxidation of coal carbonization wastewater

    SciTech Connect

    Pandey, R.A.; Handa, B.K.

    1997-01-01

    Low temperature and high temperature coal carbonization processes generate wastewaters containing ammonia, phenols, organic bases, viz. pyridine, alpha picolines, beta picolines, lutidine, quinoline and aniline. Most of the biological treatment processes employed for the treatment of the coal carbonization wastewater are evaluated and monitored for the removal of ammonia and phenols. The organic bases being pollutants of environmental concern, their status in the treatment units should be monitored. In the present investigation the fate of the organic bases has been evaluated in two stage activated sludge process employed for the treatment of coal carbonization wastewater. In the first stages of the activated sludge process, the bases, viz. pyridine, picolines, and lutidine do not get effectively removed even at high sludge retention time (SRT) of 10.9 days. The poor removal of bases in the first stage of activated sludge process unit may be attributed to the residual phenol concentration of more than 5 mg/L in the first stage of bioreactor and preferential utilization of phenols over organic bases. In the second stage of the activated sludge process most of the bases get removed effectively at SRT of 12 days. On employing a two stage activated sludge process, the bases from coal carbonization wastewaters could be removed effectively by operating the first stage at SRT of 2.18 days and the second stage of the process at 12 days SRT, respectively. 15 refs., 5 figs., 10 tabs.

  12. CONTROL OF ORGANIC SUBSTANCES IN WATER AND WASTEWATER

    EPA Science Inventory

    The presence of organic substances of industrial origin in wastewaters, storm runoff and in surface and groundwaters may not always be an unmitigated evil--but, it is safe to say, it never is good. In 1976, EPA was required to give special emphasis to 129 'priority pollutants' th...

  13. EMISSIONS OF METALS AND ORGANICS FROM MUNICIPAL WASTEWATER SLUDGE INCINERATORS

    EPA Science Inventory

    Emissions of metals and organics from a series of four wastewater sludge incinerators were determined. hree multiple hearth units and one fluidized bed combustor were tested. missions were controlled with a combination of venturi and/or tray impingement scrubbers. ne site incorpo...

  14. Detection of Organic Compounds with Whole-Cell Bioluminescent Bioassays

    PubMed Central

    Xu, Tingting; Close, Dan; Smartt, Abby; Ripp, Steven

    2015-01-01

    Natural and manmade organic chemicals are widely deposited across a diverse range of ecosystems including air, surface water, groundwater, wastewater, soil, sediment, and marine environments. Some organic compounds, despite their industrial values, are toxic to living organisms and pose significant health risks to humans and wildlife. Detection and monitoring of these organic pollutants in environmental matrices therefore is of great interest and need for remediation and health risk assessment. Although these detections have traditionally been performed using analytical chemical approaches that offer highly sensitive and specific identification of target compounds, these methods require specialized equipment and trained operators, and fail to describe potential bioavailable effects on living organisms. Alternatively, the integration of bioluminescent systems into whole-cell bioreporters presents a new capacity for organic compound detection. These bioreporters are constructed by incorporating reporter genes into catabolic or signaling pathways that are present within living cells and emit a bioluminescent signal that can be detected upon exposure to target chemicals. Although relatively less specific compared to analytical methods, bioluminescent bioassays are more cost-effective, more rapid, can be scaled to higher throughput, and can be designed to report not only the presence but also the bioavailability of target substances. This chapter reviews available bacterial and eukaryotic whole-cell bioreporters for sensing organic pollutants and their applications in a variety of sample matrices. PMID:25084996

  15. Process for removing an organic compound from water

    DOEpatents

    Baker, Richard W. (Palo Alto, CA); Kaschemekat, Jurgen (Palo Alto, CA); Wijmans, Johannes G. (Menlo Park, CA); Kamaruddin, Henky D. (San Francisco, CA)

    1993-12-28

    A process for removing organic compounds from water is disclosed. The process involves gas stripping followed by membrane separation treatment of the stripping gas. The stripping step can be carried out using one or multiple gas strippers and using air or any other gas as stripping gas. The membrane separation step can be carried out using a single-stage membrane unit or a multistage unit. Apparatus for carrying out the process is also disclosed. The process is particularly suited for treatment of contaminated groundwater or industrial wastewater.

  16. Dissolved effluent organic matter: Characteristics and potential implications in wastewater treatment and reuse applications.

    PubMed

    Michael-Kordatou, I; Michael, C; Duan, X; He, X; Dionysiou, D D; Mills, M A; Fatta-Kassinos, D

    2015-06-15

    Wastewater reuse is currently considered globally as the most critical element of sustainable water management. The dissolved effluent organic matter (dEfOM) present in biologically treated urban wastewater, consists of a heterogeneous mixture of refractory organic compounds with diverse structures and varying origin, including dissolved natural organic matter, soluble microbial products, endocrine disrupting compounds, pharmaceuticals and personal care products residues, disinfection by-products, metabolites/transformation products and others, which can reach the aquatic environment through discharge and reuse applications. dEfOM constitutes the major fraction of the effluent organic matter (EfOM) and due to its chemical complexity, it is necessary to utilize a battery of complementary techniques to adequately describe its structural and functional character. dEfOM has been shown to exhibit contrasting effects towards various aquatic organisms. It decreases metal uptake, thus potentially reducing their bioavailability to exposed organisms. On the other hand, dEfOM can be adsorbed on cell membranes inducing toxic effects. This review paper evaluates the performance of various advanced treatment processes (i.e., membrane filtration and separation processes, activated carbon adsorption, ion-exchange resin process, and advanced chemical oxidation processes) in removing dEfOM from wastewater effluents. In general, the literature findings reveal that dEfOM removal by advanced treatment processes depends on the type and the amount of organic compounds present in the aqueous matrix, as well as the operational parameters and the removal mechanisms taking place during the application of each treatment technology. PMID:25917290

  17. Use of solar distillation for olive mill wastewater drying and recovery of polyphenolic compounds.

    PubMed

    Sklavos, Sotirios; Gatidou, Georgia; Stasinakis, Athanasios S; Haralambopoulos, Dias

    2015-10-01

    Olive mill wastewater (OMW) is characterized by its high organic load and the presence of phenolic compounds. For first time, a solar distillator was used to investigate the simultaneous solar drying of OMW and the recovery of phenolic compounds with antioxidant properties in the distillate. Two experiments were conducted and the role of thermal insulation on the performance of the distiller was studied. The use of insulation resulted to higher temperatures in the distillator (up to 84.3 °C and 78.5 °C at the air and sludge, respectively), shorter period for OMW dewatering (14 days), while it increased the performance of distillator by 26.1%. Chemical characterization of the distillate showed that pH and COD concentration gradually decreased during the experiments, whereas an opposite trend was noticed for conductivity and total phenols concentration. Almost 4% of the total phenols found initially in OMW were transferred to the distillate when an insulated solar distillator was used. Gas chromatographic analysis of collected distillates confirmed the presence of tyrosol in all samples; whereas hydroxytyrosol was found only in fresh collected distillate samples. Further experiments should be conducted to optimize the process and quantify the concentrations of recovered phenolic compounds. PMID:26222602

  18. Gallic acid photochemical oxidation as a model compound of winery wastewaters.

    PubMed

    Lucas, Marco S; Dias, Albino A; Bezerra, Rui M; Peres, Jose A

    2008-09-01

    Winery wastewaters (WW) are characterized by their high organic load and by the presence of non-biodegradable compounds such as phenolic compounds. This study was undertaken to evaluate the capacity of different Advanced Oxidation Processes (AOP) combined with several radiation sources to degrade the phenolic compound Gallic Acid (GA). A toxicological assessment was also carried out to evaluate the subproduct's harmful effect generated during the most efficient AOP in the GA photoxidation. Through the course of the study it was verified that the UV radiation lamp TNN 15/32 showed the capacity to degrade 34.7% of GA, the UV radiation lamp TQ 150 achieved a value of 20.2% and the solar radiation presented only a value of 2.3% in 60 minutes. The combination of different advanced oxidation processes (Fenton's reagent, ferrioxalate and heterogeneous photocatalysis) were evaluated with the previously studied sources of radiation. From the experiments conducted it was possible to suggest that the AOP in combination with Fe(2 +) + H(2)O(2) + UV TNN 15/32 (photo-Fenton process) was the most efficient process thereby achieving the GA degradation value of 95.6% in 7.5 minutes and resulting in a total elimination of toxicity. PMID:18642152

  19. Organics and nitrogen removal from textile auxiliaries wastewater with A2O-MBR in a pilot-scale.

    PubMed

    Sun, Faqian; Sun, Bin; Hu, Jian; He, Yangyang; Wu, Weixiang

    2015-04-01

    The removal of organic compounds and nitrogen in an anaerobic-anoxic-aerobic membrane bioreactor process (A(2)O-MBR) for treatment of textile auxiliaries (TA) wastewater was investigated. The results show that the average effluent concentrations of chemical oxygen demand (COD), ammonium nitrogen (NH4(+)-N) and total nitrogen (TN) were about 119, 3 and 48 mg/L under an internal recycle ratio of 1.5. The average removal efficiency of COD, NH4(+)-N and TN were 87%, 96% and 55%, respectively. Gas chromatograph-mass spectrometer analysis indicated that, although as much as 121 different types of organic compounds were present in the TA wastewater, only 20 kinds of refractory organic compounds were found in the MBR effluent, which could be used as indicators of effluents from this kind of industrial wastewater. Scanning electron microscopy analysis revealed that bacterial foulants were significant contributors to membrane fouling. An examination of foulants components by wavelength dispersive X-ray fluorescence showed that the combination of organic foulants and inorganic compounds enhanced the formation of gel layer and thus caused membrane fouling. The results will provide valuable information for optimizing the design and operation of wastewater treatment system in the textile industry. PMID:25603291

  20. A review on the electrochemical treatment of the salty organic wastewater

    NASA Astrophysics Data System (ADS)

    Du, Xianjun

    2015-07-01

    Electrochemical technologies have proved to be useful for the treatment of wastewater, and recent years, there are growing interests in electrochemical treatment of the salty organic wastewater. The aim of this paper is to mainly present the source of the salty organic wastewater, the mechanism of direct and indirect oxidation process, and the research advances of electrochemical technologies in the salty organic wastewater by literature reports review.

  1. Organic pollution removal from coke plant wastewater using coking coal.

    PubMed

    Gao, Lihui; Li, Shulei; Wang, Yongtian; Sun, Hao

    2015-01-01

    Coke plant wastewater (CPW) is an intractable chemical wastewater, and it contains many toxic pollutants. This article presents the results of research on a semi-industrial adsorption method of coking wastewater treatment. As a sorbent, the coking coal (CC) was a dozen times less expensive than active carbon. The treatment was conducted within two scenarios, as follows: (1) adsorption after biological treatment of CPW with CC at 40 g L(-1); the chemical oxygen demand (COD) removal was 75.66%, and the concentration was reduced from 178.99 to 43.56 mg L(-1); (2) given an adsorption by CC of 250 g L(-1) prior to the biological treatment of CPW, the eliminations of COD and phenol were 58.08% and 67.12%, respectively. The CC that adsorbed organic pollution and was returned to the coking system might have no effect on both coke oven gas and coke. PMID:26114284

  2. Wastewater compounds in urban shallow groundwater wells correspond to exfiltration probabilities of nearby sewers.

    PubMed

    Lee, Do Gyun; Roehrdanz, Patrick R; Feraud, Marina; Ervin, Jared; Anumol, Tarun; Jia, Ai; Park, Minkyu; Tamez, Carlos; Morelius, Erving W; Gardea-Torresdey, Jorge L; Izbicki, John; Means, Jay C; Snyder, Shane A; Holden, Patricia A

    2015-11-15

    Wastewater compounds are frequently detected in urban shallow groundwater. Sources include sewage or reclaimed wastewater, but origins are often unknown. In a prior study, wastewater compounds were quantified in waters sampled from shallow groundwater wells in a small coastal California city. Here, we resampled those wells and expanded sample analyses to include sewage- or reclaimed water-specific indicators, i.e. pharmaceutical and personal care product chemicals or disinfection byproducts. Also, we developed a geographic information system (GIS)-based model of sanitary sewer exfiltration probability-combining a published pipe failure model accounting for sewer pipe size, age, materials of construction, with interpolated depths to groundwater-to determine if sewer system attributes relate to wastewater compounds in urban shallow groundwater. Across the wells, groundwater samples contained varying wastewater compounds, including acesulfame, sucralose, bisphenol A, 4-tert-octylphenol, estrone and perfluorobutanesulfonic acid (PFBS). Fecal indicator bacterial concentrations and toxicological bioactivities were less than known benchmarks. However, the reclaimed water in this study was positive for all bioactivity tested. Excluding one well intruded by seawater, the similarity of groundwater to sewage, based on multiple indicators, increased with increasing sanitary sewer exfiltration probability (modeled from infrastructure within ca. 300 m of each well). In the absence of direct exfiltration or defect measurements, sewer exfiltration probabilities modeled from the collection system's physical data can indicate potential locations where urban shallow groundwater is contaminated by sewage. PMID:26379202

  3. 40 CFR Table 8 to Subpart Ggg of... - Fraction Measured (Fm) for HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...2013-07-01 false Fraction Measured (Fm) for HAP Compounds in Wastewater Streams 8 Table 8 to Subpart GGG of Part 63 Protection...Part 63—Fraction Measured (Fm ) for HAP Compounds in Wastewater Streams Chemical name CAS No. a Fm Acetaldehyde...

  4. 40 CFR Table 8 to Subpart Ggg of... - Fraction Measured (Fm) for HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...2014-07-01 false Fraction Measured (Fm) for HAP Compounds in Wastewater Streams 8 Table 8 to Subpart GGG of Part 63 Protection...Part 63—Fraction Measured (Fm ) for HAP Compounds in Wastewater Streams Chemical name CAS No. a Fm Acetaldehyde...

  5. 40 CFR Table 8 to Subpart Ggg of... - Fraction Measured (Fm) for HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...2011-07-01 true Fraction Measured (Fm) for HAP Compounds in Wastewater Streams 8 Table 8 to Subpart GGG of Part 63 Protection...Part 63—Fraction Measured (Fm ) for HAP Compounds in Wastewater Streams Chemical name CAS No. a Fm Acetaldehyde...

  6. 40 CFR Table 8 to Subpart Ggg of... - Fraction Measured (Fm) for HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...Fm) for HAP Compounds in Wastewater Streams 8 Table 8 to Subpart GGG of Part...Emission Standards for Pharmaceuticals Production Pt. 63, Subpt. GGG, Table 8 Table...Fm ) for HAP Compounds in Wastewater Streams Chemical name CAS No. a Fm...

  7. 40 CFR Table 8 to Subpart Ggg of... - Fraction Measured (Fm) for HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 false Fraction Measured (Fm) for HAP Compounds in Wastewater Streams 8 Table 8 to Subpart GGG of Part 63 Protection...Part 63—Fraction Measured (Fm ) for HAP Compounds in Wastewater Streams Chemical name CAS No. a Fm Acetaldehyde...

  8. Determination of Wastewater Compounds in Whole Water by Continuous Liquid-Liquid Extraction and Capillary-Column Gas Chromatography/Mass Spectrometry

    USGS Publications Warehouse

    Zaugg, Steven D.; Smith, Steven G.; Schroeder, Michael P.

    2006-01-01

    A method for the determination of 69 compounds typically found in domestic and industrial wastewater is described. The method was developed in response to increasing concern over the impact of endocrine-disrupting chemicals on aquatic organisms in wastewater. This method also is useful for evaluating the effects of combined sanitary and storm-sewer overflow on the water quality of urban streams. The method focuses on the determination of compounds that are indicators of wastewater or have endocrine-disrupting potential. These compounds include the alkylphenol ethoxylate nonionic surfactants, food additives, fragrances, antioxidants, flame retardants, plasticizers, industrial solvents, disinfectants, fecal sterols, polycyclic aromatic hydrocarbons, and high-use domestic pesticides. Wastewater compounds in whole-water samples were extracted using continuous liquid-liquid extractors and methylene chloride solvent, and then determined by capillary-column gas chromatography/mass spectrometry. Recoveries in reagent-water samples fortified at 0.5 microgram per liter averaged 72 percent ? 8 percent relative standard deviation. The concentration of 21 compounds is always reported as estimated because method recovery was less than 60 percent, variability was greater than 25 percent relative standard deviation, or standard reference compounds were prepared from technical mixtures. Initial method detection limits averaged 0.18 microgram per liter. Samples were preserved by adding 60 grams of sodium chloride and stored at 4 degrees Celsius. The laboratory established a sample holding-time limit prior to sample extraction of 14 days from the date of collection.

  9. Photoassisted Biodegradation of Irradiated Organics in Simulated Nuclear Wastewater.

    PubMed

    Makgato, Stanford S; Nkhalambayausi-Chirwa, Evans M

    2015-05-01

    The extent of dehalogenation and degradation of toxic aromatic compounds in a nuclear wastewater was evaluated using a two-stage system consisting of a photolytic reactor followed by a biological reactor. Experiments were performed by varying the initial 4-chlorophenol (4-CP) concentration from 50 to 1000 mg/L. The UV pretreatment stage improved the overall efficiency of biodegradation of the recalcitrant compound by facilitating degradability in the biological stage. Removal efficiencies greater than 98% were achieved at 4-CP feed concentrations < 50 mg/L. Adding an H2O2 dose of 0.1 mg/L as an oxidant further improved biodegradation under optimum operating conditions for the entire system. Some known aromatic compound degraders such as Pseudomonas aeruginosa and Pseudomonas mendocina were detected in the consortium using the 16S rRNA genetic fingerprint technique. To the authors' knowledge, this is the first study on biodegradation of halogenated aromatic compounds that are copollutants of metallic radionuclides in radioactive wastewater. PMID:26460459

  10. Methods of making organic compounds by metathesis

    DOEpatents

    Abraham, Timothy W.; Kaido, Hiroki; Lee, Choon Woo; Pederson, Richard L.; Schrodi, Yann; Tupy, Michael John

    2015-09-01

    Described are methods of making organic compounds by metathesis chemistry. The methods of the invention are particularly useful for making industrially-important organic compounds beginning with starting compositions derived from renewable feedstocks, such as natural oils. The methods make use of a cross-metathesis step with an olefin compound to produce functionalized alkene intermediates having a pre-determined double bond position. Once isolated, the functionalized alkene intermediate can be self-metathesized or cross-metathesized (e.g., with a second functionalized alkene) to produce the desired organic compound or a precursor thereto. The method may be used to make bifunctional organic compounds, such as diacids, diesters, dicarboxylate salts, acid/esters, acid/amines, acid/alcohols, acid/aldehydes, acid/ketones, acid/halides, acid/nitriles, ester/amines, ester/alcohols, ester/aldehydes, ester/ketones, ester/halides, ester/nitriles, and the like.

  11. SITE TECHNOLOGY CAPSULE: ZENOGEM™ WASTEWATER TREATMENT PROCESS

    EPA Science Inventory

    Zenon Environmental System's ZenoGem™ Wastewater Treatment Process treats aqueous media contaminated with volatile/semi-volatile organic compounds. This technology combines aerobic biological treatment to remove biodegradable organic compounds with ultrafiltration to separate res...

  12. SORPTION OF HYDROPHOBIC ORGANIC COMPOUNDS BY SEDIMENTS

    EPA Science Inventory

    Thermodynamic and kinetic principles which govern the uptake of nonionic, hydrophobic organic chemicals by sediments in aqueous systems are summarized. Sorption onto organic-rich sediments can be modeled as a process where the hydrophobic compound partitions into the organic matt...

  13. Occurrence of organic wastewater contaminants, pharmaceuticals, and personal care products in selected water supplies, Cape Cod, Massachusetts, June 2004

    USGS Publications Warehouse

    Zimmerman, Marc J.

    2005-01-01

    In June 2004, the U.S. Geological Survey, in cooperation with the Barnstable County Department of Health and Environment, sampled water from 14 wastewater sources and drinking-water supplies on Cape Cod, Massachusetts, for the presence of organic wastewater contaminants, pharmaceuticals, and personal care products. The geographic distribution of sampling locations does not represent the distribution of drinking-water supplies on Cape Cod. The environmental presence of the analyte compounds is mostly unregulated; many of the compounds are suspected of having adverse ecological and human health effects. Of the 85 different organic analyte compounds, 43 were detected, with 13 detected in low concentrations (less than 1 microgram per liter) from drinking-water supplies thought to be affected by wastewater because of previously detected high nitrate concentrations. (Phenol and d-limonene, detected in equipment blanks at unacceptably high concentrations, are not included in counts of detections in this report.) Compounds detected in the drinking-water supplies included the solvent, tetrachloroethylene; the analgesic, acetaminophen; the antibiotic, sulfamethoxazole; and the antidepressant, carbamazapine. Nitrate nitrogen, an indicator of wastewater, was detected in water supplies in concentrations ranging from 0.2 to 8.8 milligrams per liter.

  14. DEVELOPMENT AND EVALUATION OF METHODS FOR TOTAL ORGANIC HALIDE AND PURGEABLE ORGANIC HALIDE IN WASTEWATER

    EPA Science Inventory

    This report describes a series of studies involving the use of 'surrogate' methods for the determination of total organic halides (TOX), purgeable organic halides (POX), and solvent extractable organic halides (EOX), in wastewater and solid wastes. A pyrolysis/microcoulometric sy...

  15. Thermodynamic properties of organic iodine compounds

    NASA Astrophysics Data System (ADS)

    Richard, Laurent; Gaona, Xavier

    2011-11-01

    A critical evaluation has been made of the thermodynamic properties reported in the literature for 43 organic iodine compounds in the solid, liquid, or ideal gas state. These compounds include aliphatic, cyclic and aromatic iodides, iodophenols, iodocarboxylic acids, and acetyl and benzoyl iodides. The evaluation has been made on the basis of carbon number systematics and group additivity relations, which also allowed to provide estimates of the thermodynamic properties of those compounds for which no experimental data were available. Standard molal thermodynamic properties at 25 °C and 1 bar and heat capacity coefficients are reported for 13 crystalline, 29 liquid, and 39 ideal gas organic iodine compounds, which can be used to calculate the corresponding properties as a function of temperature and pressure. Values derived for the standard molal Gibbs energy of formation at 25 °C and 1 bar of these crystalline, liquid, and ideal gas organic iodine compounds have subsequently been combined with either solubility measurements or gas/water partition coefficients to obtain values for the standard partial molal Gibbs energies of formation at 25 °C and 1 bar of 32 aqueous organic iodine compounds. The thermodynamic properties of organic iodine compounds calculated in the present study can be used together with those for aqueous inorganic iodine species to predict the organic/inorganic speciation of iodine in marine sediments and petroleum systems, or in the near- and far-field of nuclear waste repositories.

  16. Organic electronic devices using phthalimide compounds

    DOEpatents

    Hassan, Azad M.; Thompson, Mark E.

    2013-03-19

    Organic electronic devices comprising a phthalimide compound. The phthalimide compounds disclosed herein are electron transporters with large HOMO-LUMO gaps, high triplet energies, large reduction potentials, and/or thermal and chemical stability. As such, these phthalimide compounds are suitable for use in any of various organic electronic devices, such as OLEDs and solar cells. In an OLED, the phthalimide compounds may serve various functions, such as a host in the emissive layer, as a hole blocking material, or as an electron transport material. In a solar cell, the phthalimide compounds may serve various functions, such as an exciton blocking material. Various examples of phthalimide compounds which may be suitable for use in the present invention are disclosed.

  17. Organic electronic devices using phthalimide compounds

    DOEpatents

    Hassan, Azad M.; Thompson, Mark E.

    2012-10-23

    Organic electronic devices comprising a phthalimide compound. The phthalimide compounds disclosed herein are electron transporters with large HOMO-LUMO gaps, high triplet energies, large reduction potentials, and/or thermal and chemical stability. As such, these phthalimide compounds are suitable for use in any of various organic electronic devices, such as OLEDs and solar cells. In an OLED, the phthalimide compounds may serve various functions, such as a host in the emissive layer, as a hole blocking material, or as an electron transport material. In a solar cell, the phthalimide compounds may serve various functions, such as an exciton blocking material. Various examples of phthalimide compounds which may be suitable for use in the present invention are disclosed.

  18. Organic electronic devices using phthalimide compounds

    DOEpatents

    Hassan, Azad M.; Thompson, Mark E.

    2010-09-07

    Organic electronic devices comprising a phthalimide compound. The phthalimide compounds disclosed herein are electron transporters with large HOMO-LUMO gaps, high triplet energies, large reduction potentials, and/or thermal and chemical stability. As such, these phthalimide compounds are suitable for use in any of various organic electronic devices, such as OLEDs and solar cells. In an OLED, the phthalimide compounds may serve various functions, such as a host in the emissive layer, as a hole blocking material, or as an electron transport material. In a solar cell, the phthalimide compounds may serve various functions, such as an exciton blocking material. Various examples of phthalimide compounds which may be suitable for use in the present invention are disclosed.

  19. High organic loading treatment for industrial molasses wastewater and microbial community shifts corresponding to system development.

    PubMed

    Kuroda, Kyohei; Chosei, Tomoaki; Nakahara, Nozomi; Hatamoto, Masashi; Wakabayashi, Takashi; Kawai, Toshikazu; Araki, Nobuo; Syutsubo, Kazuaki; Yamaguchi, Takashi

    2015-11-01

    Molasses wastewater contains high levels of organic compounds, cations, and anions, causing operational problems for anaerobic biological treatment. To establish a high organic loading treatment system for industrial molasses wastewater, this study designed a combined system comprising an acidification tank, a thermophilic multi-stage (MS)-upflow anaerobic sludge blanket (UASB) reactor, mesophilic UASB reactor, and down-flow hanging sponge reactor. The average total chemical oxygen demand (COD) and biochemical oxygen demand removal rates were 85%±3% and 95%±2%, respectively, at an organic loading rate of 42kgCODcrm(-3)d(-1) in the MS-UASB reactor. By installation of the acidification tank, the MS-UASB reactor achieved low H2-partial pressure. The abundance of syntrophs such as fatty acid-degrading bacteria increased in the MS-UASB and 2nd-UASB reactors. Thus, the acidification tank contributed to maintaining a favorable environment for syntrophic associations. This study provides new information regarding microbial community composition in a molasses wastewater treatment system. PMID:26241842

  20. Integration of wet oxidation and nanofiltration for treatment of recalcitrant organics in wastewater

    SciTech Connect

    Hellenbrand, R.; Mantzavinos, D.; Metcalfe, I.S.; Livingston, A.G.

    1997-12-01

    Wet oxidation and nanofiltration are employed in an integrated system for the treatment of bioresistant industrial wastewaters. The partial oxidation products formed during a brief period of pretreatment in a low pressure WO reactor are separated by nanofiltration, and larger molecules are recycled into the reactor where they undergo further oxidation. Experiments were carried out with polyethylene glycol as a model compound in aqueous solution, representing polymer manufacture wastewater. The results demonstrate that by using a combination of an oxidative and a separative step, a higher selectivity of the overall process toward partial oxidation can be achieved. The permeate leaving the filtration step is mainly composed of short chain organic acids which could be readily biodegraded in a subsequent biological treatment, or discharged if concentrations are low.

  1. INVESTIGATIONS OF BIODEGRADABILITY AND TOXICITY OF ORGANIC COMPOUNDS

    EPA Science Inventory

    The development of elaborate industrial societies has led to proliferation of a vast number of complex chemicals for industrial, agricultural and domestic use. Some portion of these compounds eventually find their way into municipal and industrial wastewater. Unless specifically ...

  2. Biodegradability of wastewater and activated sludge organics in anaerobic digestion.

    PubMed

    Ikumi, D S; Harding, T H; Ekama, G A

    2014-06-01

    The investigation provides experimental evidence that the unbiodegradable particulate organics fractions of primary sludge and waste activated sludge calculated from activated sludge models remain essentially unbiodegradable in anaerobic digestion. This was tested by feeding the waste activated sludge (WAS) from three different laboratory activated sludge (AS) systems to three separate anaerobic digesters (AD). Two of the AS systems were Modified Ludzack - Ettinger (MLE) nitrification-denitrification (ND) systems and the third was a membrane University of Cape Town (UCT) ND and enhanced biological P removal system. One of the MLE systems and the UCT system were fed the same real settled wastewater. The other MLE system was fed raw wastewater which was made by adding a measured constant flux (gCOD/d) of macerated primary sludge (PS) to the real settled wastewater. This PS was also fed to a fourth AD and a blend of PS and WAS from settled wastewater MLE system was fed to a fifth AD. The five ADs were each operated at five different sludge ages (10-60d). From the measured performance results of the AS systems, the unbiodegradable particulate organic (UPO) COD fractions of the raw and settled wastewaters, the PS and the WAS from the three AS systems were calculated with AS models. These AS model based UPO fractions of the PS and WAS were compared with the UPO fractions calculated from the performance results of the ADs fed these sludges. For the PS, the UPO fraction calculated from the AS and AD models matched closely, i.e. 0.30 and 0.31. Provided the UPO of heterotrophic (OHO, fE_OHO) and phosphorus accumulating (PAO, fE_PAO) biomass were accepted to be those associated with the death regeneration model of organism "decay", the UPO of the WAS calculated from the AS and AD models also matched well - if the steady state AS model fE_OHO = 0.20 and fE_PAO = 0.25 values were used, then the UPO fraction of the WAS calculated from the AS models deviated significantly from those calculated with the AD models. Therefore in plant wide wastewater treatment models the characterization of PS and WAS as defined by the AS models can be applied without modification in AD models. The observed rate limiting hydrolysis/acidogenesis rates of the sludges are listed. PMID:24699419

  3. Microwave spectra of some volatile organic compounds

    NASA Technical Reports Server (NTRS)

    White, W. F.

    1975-01-01

    A computer-controlled microwave (MRR) spectrometer was used to catalog reference spectra for chemical analysis. Tables of absorption frequency, peak absorption intensity, and integrated intensity are included for 26 volatile organic compounds, all but one of which contain oxygen.

  4. VOLATILE ORGANIC COMPOUNDS AS EXPOSURE BIOMARKERS

    EPA Science Inventory

    Alveolar breath sampling and analysis can be extremely useful in exposure assessment studies involving volatile organic compounds (VOCs). Over recent years scientists from the US Environmental Protection Agency's National Exposure Research Laboratory have developed and refined...

  5. PERFLUORINATED ORGANIC COMPOUND EXPOSURE ASSESSMENT RESEARCH

    EPA Science Inventory

    A wide range of perfluorinated organic compounds (PFCs) has been used in a variety of industrial processes and consumer products. The most commonly studied PFCs include perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA), but there are many more compounds in this c...

  6. (CHINA) PERFLUORINATED ORGANIC COMPOUND EXPOSURE ASSESSMENT RESEARCH

    EPA Science Inventory

    A wide range of perfluorinated organic compounds (PFCs) has been used in a variety of industrial processes and consumer products. The most commonly studied PFCs include perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA), but there are many more compounds in this c...

  7. Volatile organic compound emissions from silage systems

    Technology Transfer Automated Retrieval System (TEKTRAN)

    As a precursor to smog, emission of volatile organic compounds (VOCs) to the atmosphere is an environmental concern in some regions. The major source from farms is silage, with emissions coming from the silo face, mixing wagon, and feed bunk. The major compounds emitted are alcohols with other impor...

  8. VOLATILE ORGANIC COMPOUNDS (VOCS) CHAPTER 31.

    EPA Science Inventory

    The term "volatile organic compounds' (VOCs) was originally coined to refer, as a class, to carbon-containing chemicals that participate in photochemical reactions in the ambient (outdoor) are. The regulatory definition of VOCs used by the U.S. EPA is: Any compound of carbon, ex...

  9. Alkylation of organic aromatic compounds

    DOEpatents

    Smith, Jr., Lawrence A. (Bellaire, TX); Arganbright, Robert P. (Seabrook, TX); Hearn, Dennis (Houston, TX)

    1994-01-01

    Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C.sub.2 to C.sub.10 olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80.degree. C. to 500.degree. C., using as the catalyst a mole sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene below the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms.

  10. Alkylation of organic aromatic compounds

    DOEpatents

    Smith, Jr., Lawrence A. (Houston, TX)

    1989-01-01

    Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C.sub.2 to C.sub.10 olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80.degree. C. to 500.degree. C., using as the catalyst a mole sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene below the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms.

  11. Alkylation of organic aromatic compounds

    DOEpatents

    Smith, L.A. Jr.; Arganbright, R.P.; Hearn, D.

    1994-06-14

    Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C[sub 2] to C[sub 10] olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80 C to 500 C, using as the catalyst a molecular sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene below the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms. 1 fig.

  12. Alkylation of organic aromatic compounds

    DOEpatents

    Smith, L.A. Jr.

    1989-07-18

    Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C[sub 2] to C[sub 10] olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80 C to 500 C, using as the catalyst a mole sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene below the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms. 1 fig.

  13. Alkylation of organic aromatic compounds

    DOEpatents

    Smith, Jr., Lawrence A. (Bellaire, TX); Arganbright, Robert P. (Seabrook, TX); Hearn, Dennis (Houston, TX)

    1993-01-01

    Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C.sub.2 to C.sub.10 olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80.degree. C. to 500.degree. C., using as the catalyst a mole sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene to about the mid point of the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms.

  14. Alkylation of organic aromatic compounds

    DOEpatents

    Smith, L.A. Jr.; Arganbright, R.P.; Hearn, D.

    1993-09-07

    Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C[sub 2] to C[sub 10] olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80 C to 500 C, using as the catalyst a molecular sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene to about the mid point of the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms. 1 figures.

  15. Identification and quantification of volatile organic compounds from a dairy

    NASA Astrophysics Data System (ADS)

    Filipy, Jenny; Rumburg, Brian; Mount, George; Westberg, Hal; Lamb, Brian

    Volatile organic compounds (VOCs) that contribute to odor and air quality problems have been identified from the Washington State University Knott Dairy Farm using gas chromatography-mass spectroscopy (GC-MS). Eighty-two VOCs were identified at a lactating cow open stall and 73 were detected from a slurry wastewater lagoon. These compounds included alcohols, aldehydes, ketones, esters, ethers, aromatic hydrocarbons, halogenated hydrocarbons, terpenes, other hydrocarbons, amines, other nitrogen containing compounds, and sulfur-containing compounds. The concentration of VOCs directly associated with cattle waste increased with ambient air temperature, with the highest concentrations present during the summer months. Concentrations of most detected compounds were below published odor detection thresholds. Emission rates of ethanol (1026±513 ?g cow -1 s -1) and dimethyl sulfide (DMS) (13.8±10.3 ?g cow -1 s -1) were measured from the lactating stall area using an atmospheric tracer method and concentrations were plotted using data over a 2-year period. Emission rates of acetone (3.03±0.85 ng cow -1 s -1), 2-butanone (145±35 ng cow -1 s -1), methyl isobutyl ketone (3.46±1.11 ng cow -1 s -1), 2-methyl-3-pentanone (25.1±8.0 ng cow -1 s -1), DMS (2.19±0.92 ng cow -1 s -1), and dimethyl disulfide (DMDS) (16.1±3.9 ng cow -1 s -1) were measured from the slurry waste lagoon using a laboratory emission chamber.

  16. Alkylation of organic aromatic compounds

    DOEpatents

    Smith, Jr., Lawrence A. (Bellaire, TX); Arganbright, Robert P. (Seabrook, TX); Hearn, Dennis (Houston, TX)

    1993-01-01

    Aromatic compounds are alkylated in a combination reactor/distillation column comprising a vessel suitable for operating between 70.degree. C. and 500.degree. C. and from 0.5 to 20 atmospheres pressure; an inert distillation packing in the lower one-third of said vessel; solid acidic catalytic material such as zeolites or an acidic cation exchange resin supported in the middle one-third of said vessel; and inert distillation packing in the upper one-third of said vessel. A benzene inlet is located near the upper end of the vessel; an olefin inlet is juxtaposed with said solid acidic catalytic material; a bottoms outlet is positioned near the bottom of said vessel for removing said cumene and ethyl benzene; and an overhead outlet is placed at the top of said vessel for removing any unreacted benzene and olefin.

  17. Alkylation of organic aromatic compounds

    DOEpatents

    Smith, L.A. Jr.; Arganbright, R.P.; Hearn, D.

    1993-01-05

    Aromatic compounds are alkylated in a combination reactor/distillation column comprising a vessel suitable for operating between 70 C and 500 C and from 0.5 to 20 atmospheres pressure; an inert distillation packing in the lower one-third of said vessel; solid acidic catalytic material such as zeolites or an acidic cation exchange resin supported in the middle one-third of said vessel; and inert distillation packing in the upper one-third of said vessel. A benzene inlet is located near the upper end of the vessel; an olefin inlet is juxtaposed with said solid acidic catalytic material; a bottoms outlet is positioned near the bottom of said vessel for removing said cumene and ethyl benzene; and an overhead outlet is placed at the top of said vessel for removing any unreacted benzene and olefin.

  18. Acid characteristics of dissolved organic matter in wastewater

    SciTech Connect

    Wang, J.; Huang, C.P.; Allen, H.E.; Takiyama, L.R.; Poesponegoro, I.; Poesponegoro, H.; Pirestani, D.

    1998-07-01

    The presence of dissolved organic matter (DOM) in a wastewater treatment system can significantly affect the uptake of heavy metals by sludge particulates. The characteristics of DOM, its concentration, and the solution pH are important parameters governing the heavy metals uptake reaction. The characteristics of DOM of various wastewater and sludge (primary, secondary, and tertiary) samples collected from four municipal wastewater treatment plants were investigated. Results showed that the dissolution of DOM from sludge is significantly affected by pH and suspended solids concentration. Results also showed that DOM contains two discrete acid groups that are available for metals complexation. The site concentration and acidity constants were determined by an alkalimetric titration method. For all DOM samples studied, the acidity constants, pK{sub aA} and pK{sub aB}, were 5.3 and 9.5, respectively. Based on the acidity constants and the Fourier transform infrared spectra, it is believed that the acid sites consist of carboxylic and amino functional groups. The density of the first acid site was approximately 10{sup {minus}5} mol/mg chemical oxygen demand for all samples studied. However, the density of the second acid site varied significantly among the DOM samples investigated.

  19. Occurrence of organic wastewater and other contaminants in cave streams in northeastern Oklahoma and northwestern Arkansas

    USGS Publications Warehouse

    Bidwell, Joseph R.; Becker, C.; Hensley, S.; Stark, R.; Meyer, M.T.

    2010-01-01

    The prevalence of organic wastewater compounds in surface waters of the United States has been reported in a number of recent studies. In karstic areas, surface contaminants might be transported to groundwater and, ultimately, cave ecosystems, where they might impact resident biota. In this study, polar organic chemical integrative samplers (POCISs) and semipermeable membrane devices (SPMDs) were deployed in six caves and two surface-water sites located within the Ozark Plateau of northeastern Oklahoma and northwestern Arkansas in order to detect potential chemical contaminants in these systems. All caves sampled were known to contain populations of the threatened Ozark cavefish (Amblyopsis rosae). The surface-water site in Oklahoma was downstream from the outfall of a municipal wastewater treatment plant and a previous study indicated a hydrologic link between this stream and one of the caves. A total of 83 chemicals were detected in the POCIS and SPMD extracts from the surface-water and cave sites. Of these, 55 chemicals were detected in the caves. Regardless of the sampler used, more compounds were detected in the Oklahoma surface-water site than in the Arkansas site or the caves. The organic wastewater chemicals with the greatest mass measured in the sampler extracts included sterols (cholesterol and ??-sitosterol), plasticizers [diethylhexylphthalate and tris (2-butoxyethyl) phosphate], the herbicide bromacil, and the fragrance indole. Sampler extracts from most of the cave sites did not contain many wastewater contaminants, although extracts from samplers in the Oklahoma surfacewater site and the cave hydrologically linked to it had similar levels of diethylhexyphthalate and common detections of carbamazapine, sulfamethoxazole, benzophenone, N-diethyl-3-methylbenzamide (DEET), and octophenol monoethoxylate. Further evaluation of this system is warranted due to potential ongoing transport of wastewaterassociated chemicals into the cave. Halogenated organics found in caves and surface-water sites included brominated flame retardants, organochlorine pesticides (chlordane and nonachlor), and polychlorinated biphenyls. The placement of samplers in the caves (near the cave mouth compared to farther in the system) might have influenced the number of halogenated organics detected due to possible aerial transport of residues. Guano from cave-dwelling bats also might have been a source of some of these chlorinated organics. Seven-day survival and growth bioassays with fathead minnows (Pimephales promelas) exposed to samples of cave water indicated initial toxicity in water from two of the caves, but these effects were transient, with no toxicity observed in follow-up tests. ??Springer Science+Business Media, LLC 2009.

  20. Reflectance spectroscopy of organic compounds: 1. Alkanes

    USGS Publications Warehouse

    Clark, R.N.; Curchin, J.M.; Hoefen, T.M.; Swayze, G.A.

    2009-01-01

    Reflectance spectra of the organic compounds comprising the alkane series are presented from the ultraviolet to midinfrared, 0.35 to 15.5 /??m. Alkanes are hydrocarbon molecules containing only single carbon-carbon bonds, and are found naturally on the Earth and in the atmospheres of the giant planets and Saturn's moon, Titan. This paper presents the spectral properties of the alkanes as the first in a series of papers to build a spectral database of organic compounds for use in remote sensing studies. Applications range from mapping the environment on the Earth, to the search for organic molecules and life in the solar system and throughout the. universe. We show that the spectral reflectance properties of organic compounds are rich, with major diagnostic spectral features throughout the spectral range studied. Little to no spectral change was observed as a function of temperature and only small shifts and changes in the width of absorption bands were observed between liquids and solids, making remote detection of spectral properties throughout the solar system simpler. Some high molecular weight organic compounds contain single-bonded carbon chains and have spectra similar to alkanes even ' when they fall into other families. Small spectral differences are often present allowing discrimination among some compounds, further illustrating the need to catalog spectral properties for accurate remote sensing identification with spectroscopy.

  1. Catalyst for Oxidation of Volatile Organic Compounds

    NASA Technical Reports Server (NTRS)

    Wood, George M. (Inventor); Upchurch, Billy T. (Inventor); Schryer, David R. (Inventor); Davis, Patricia P. (Inventor); Kielin, Erik J. (Inventor); Brown, Kenneth G. (Inventor); Schyryer, Jacqueline L. (Inventor); DAmbrosia, Christine M. (Inventor)

    2000-01-01

    Disclosed is a process for oxidizing volatile organic compounds to carbon dioxide and water with the minimal addition of energy. A mixture of the volatile organic compound and an oxidizing agent (e.g. ambient air containing the volatile organic compound) is exposed to a catalyst which includes a noble metal dispersed on a metal oxide which possesses more than one oxidation state. Especially good results are obtained when the noble metal is platinum, and the metal oxide which possesses more than one oxidation state is tin oxide. A promoter (i.e., a small amount of an oxide of a transition series metal) may be used in association with the tin oxide to provide very beneficial results.

  2. Organic pollutants removal in wastewater by heterogeneous photocatalytic ozonation.

    PubMed

    Xiao, Jiadong; Xie, Yongbing; Cao, Hongbin

    2015-02-01

    Heterogeneous photocatalysis and ozonation are robust advanced oxidation processes for eliminating organic contaminants in wastewater. The combination of these two methods is carried out in order to enhance the overall mineralization of refractory organics. An apparent synergism between heterogeneous photocatalysis and ozonation has been demonstrated in many literatures, which gives rise to an improvement of total organic carbon removal. The present overview dissects the heterogeneous catalysts and the influences of different operational parameters, followed by the discussion on the kinetics, mechanism, economic feasibility and future trends of this integrated technology. The enhanced oxidation rate mainly results from a large amount of hydroxyl radicals generated from a synergistically induced decomposition of dissolved ozone, besides superoxide ion radicals and the photo-induced holes. Six reaction pathways possibly exist for the generation of hydroxyl radicals in the reaction mechanism of heterogeneous photocatalytic ozonation. PMID:25479808

  3. Treatment of organic-heavy metal wastewaters using granular activated carbon (GAC) columns

    SciTech Connect

    Reed, B.E.; Jamil, M.; Carriere, P.; Thomas, B.

    1995-12-31

    In the past, granular activated carbon (GAC) columns have been used to remove trace amounts of organic compounds from various aqueous waste streams. If heavy metals were present, other processes such as precipitation, reverse osmosis, or ion exchange would be added to the treatment flow sheet. Significant savings could result if organic-heavy metal wastewaters could be successfully treated using a single process. Researchers at West Virginia University in conjunction with Norit Americas, Inc. have recently developed a GAC column process that removes heavy metals from the aqueous phase using GAC columns. Because the ability of using GAC columns to remove organic contaminants is well known, the next logical step is to demonstrate the feasibility of the GAC process to simultaneously remove organic and inorganic contaminants. In this study, two synthetic wastewaters, 1 mg/L Pb-10 mg/L phenol and 1 mg/L Pb-1 mg/L TCE, were treated by GAC columns containing the Norit Americas, Inc. carbon Hydrodarco (HD) 4000.

  4. Occurrence of pharmaceutically active and non-steroidal estrogenic compounds in three different wastewater recycling schemes in Australia 

    E-print Network

    Al-Rifai, Jawad H.; Gabelish, Candace L.; Schäfer, Andrea

    2007-01-01

    The discovery that natural and synthetic chemicals, in the form of excreted hormones and pharmaceuticals, as well as a vast array of compounds with domestic and industrial applications, can enter the environment via wastewater treatment plants...

  5. [Kinetic analysis of laccase catalyze phenolic and aniline compounds and detecting catechol in wastewater].

    PubMed

    Zhong, Ping-Fang; Peng, Hui-Min; Peng, Fang-Yi; Cai, Qiang; He, Miao

    2010-11-01

    Phenolic or aniline compounds were important pollutants in the industrial wastewaters to seriously polluted water environment. This research developed a detecting method of phenolic and aniline compounds based on the kinetic parameters of the substrates of laccase. Catalytic reaction between laccase and phenolic and aniline compounds was characterized using spectrophotometic method, which resulted 0-10 mg/L substrate reaction rate and calibration curve of substrate concentration and reaction rate. And then the non-volatile phenols in three kinds of coking wastewater were screened and the contents were detected. The result showed that polyhydric phenol, multi-amine and aminophenol were the main substrates of laccase. The optimum pH of phenols was around 7.0 and anilines 4.5-5.0, K(m) values of each substrates was 0.4-10 mmol/L. The calibration curve performed good first order kinetics linear relationship except benzidine with correlation coefficients above 0.96. Using laccase method, the contents of catechol in three kinds of coking wastewater were respectively detected to be 190.5, 265.8 and 155.3 mg/L with recoveries ranged from 89.9% to 115.8%. PMID:21250450

  6. Review on the occurrence, fate and removal of perfluorinated compounds during wastewater treatment.

    PubMed

    Arvaniti, Olga S; Stasinakis, Athanasios S

    2015-08-15

    Perfluorinated compounds (PFCs) consist of a fully fluorinated hydrophobic alkyl chain attached to a hydrophilic end group. Due to their wide use in several industrial and household applications, they have been detected in numerous Sewage Treatment Plants (STPs) during the last ten years. The present review reports the occurrence of 22 PFCs (C4-C14, C16, C18 carboxylates; C4-C8 and C10 sulfonates; 3 sulfonamides) in municipal or/and industrial wastewater, originating from 24 monitoring studies. PFCs levels in sewage sludge have also been reported using data from 12 studies. Most of the above monitoring data originate from the USA, North Europe and Asia and concern perfluorooctanesulfonate (PFOS) and perfluorooctanoic acid (PFOA), while limited information is available from Mediterranean area, Canada and Australia. PFCs concentrations range up to some hundreds ng/L and some thousands ng/g dry weight in raw wastewater and sludge, respectively. They are not significantly removed during secondary biological treatment, while their concentrations in treated wastewater are often higher compared to raw sewage. Their biodegradation during wastewater treatment does not seem possible; whereas some recent studies have noted the potential transformation of precursor compounds to PFCs during biological wastewater treatment. PFCs sorption onto sludge has been studied in depth and seems to be an important mechanism governing their removal in STPs. Concerning tertiary treatment technologies, significant PFCs removal has been observed using activated carbon, nanofiltration, reverse osmosis or applying advanced oxidation and reduction processes. Most of these studies have been conducted using pure water, while in many cases the experiments have been performed under extreme laboratory conditions (high concentrations, high radiation source, temperature or pressure). Future efforts should be focused on better understanding of biotransformation processes occurred in aerobic and anaerobic bioreactors and result to PFCs formation and on the application of advanced treatment technologies under conditions commonly found in STPs. PMID:25889547

  7. Separation of volatile organic compounds by pervaporation for a binary compound combination: Trichloroethylene and 1,1,1-trichloroethane

    SciTech Connect

    Visvanathan, C.; Basu, B.; Mora, J.C.

    1995-11-01

    This study evaluates the behavior of sweeping air pervaporation when used to separate trichloroethylene (TCE) and 1,1,1-trichloroethane (TCEthane) from wastewater. Selectivity and membrane preference are studied. Models for binary compounds are studied to evaluate the extent of cross influence on TCE flux due to the presence of another volatile organic compound, TCEthane. Using the models, the integral dry diffusion coefficient for TCEthane is evaluated. Results indicate that the membrane exhibits a preference for TCE over TCEthane. However, the values of the diffusion rates are found to be comparable. Selectivity values are found to be independent of the air flow rate but dependent on the relative concentration of the compounds in the feed solution. It is found that, due to the presence of TCEthane, the flux of TCE decreased. Further, it is found that the ratio of the integral dry diffusion coefficients of the compounds is inversely proportional to the ratio of their molecular weights.

  8. Sorption capacity of ground tires for vapor-phase volatile organic compounds

    SciTech Connect

    Kim, J.Y.; Park, J.K.; Edil, T.B.; Jhung, J.K.

    1996-12-31

    Batch sorption tests were conducted to determine the partition coefficient of volatile organic compounds (VOCs) by ground tires. The partition coefficient in the vapor phase was estimated by dividing the partition coefficient in the aqueous phase by Henry`s law constant. Under a diluted condition VOCs are sorbed onto ground tires noncompetitively regardless of the existence of other VOCs. Polar compounds such as methylene chloride were less sorbed onto ground tires than nonpolar compounds. The vapor-phase partition coefficient was found to have a logarithmic relationship with the saturation vapor concentration. VOCs emitted from waste-water treatment facilities can be effectively retarded by the ground tires.

  9. Comparative Toxicity of Chlorinated Saline and Freshwater Wastewater Effluents to Marine Organisms.

    PubMed

    Yang, Mengting; Liu, Jiaqi; Zhang, Xiangru; Richardson, Susan D

    2015-12-15

    Toilet flushing with seawater results in saline wastewater, which may contain approximately 33-50% seawater. Halogenated disinfection byproducts (DBPs), especially brominated and iodinated DBPs, have recently been found in chlorinated saline wastewater effluents. With the occurrence of brominated and iodinated DBPs, the adverse effects of chlorinated saline wastewater effluents to marine ecology have been uncertain. By evaluating the developmental effects in the marine polychaete Platynereis dumerilii directly exposed to chlorinated saline/freshwater wastewater effluents, we found surprisingly that chlorinated saline wastewater effluents were less toxic than a chlorinated freshwater wastewater effluent. This was also witnessed by the marine alga Tetraselmis marina. The toxicity of a chlorinated wastewater effluent to the marine species was dominated by its relatively low salinity compared to the salinity in seawater. The organic matter content in a chlorinated wastewater effluent might be partially responsible for the toxicity. The adverse effects of halogenated DBPs on the marine species were observed pronouncedly only in the "concentrated" chlorinated wastewater effluents. pH and ammonia content in a wastewater effluent caused no adverse effects on the marine species. The results suggest that using seawater to replace freshwater for toilet flushing might mitigate the "direct" acute detrimental effect of wastewater to the marine organisms. PMID:26505276

  10. Emission characteristics and factors of selected odorous compounds at a wastewater treatment plant.

    PubMed

    Jeon, Eui-Chan; Son, Hyun-Keun; Sa, Jae-Hwan

    2009-01-01

    THIS STUDY WAS INITIATED TO EXPLORE THE EMISSION CHARACTERISTICS OF REDUCED SULFUR COMPOUNDS (RSCS: hydrogen sulfide, methyl mercaptan, dimethyl sulfide, dimethyl disulfide), ammonia and trimethylamine from a Wastewater Treatment Plant (WWTP) located at Sun-Cheon, Chonlanam-Do in South Korea. The study also evaluates flux profiles of the six selected odorous compounds and their flux rates (?g/m(2)/min) and compares their emission characteristics. A Dynamic Flux Chamber DFC was used to measure fluxes of pollutants from the treatment plant. Quality control of odor samples using a non-reactive sulfur dioxide gas determined the time taken for DFC concentration to reach equilibrium. The reduced sulfur compounds were analyzed by interfacing gas chromatography with a Pulsed Flame Photometric Detector (PFPD). Air samples were collected in the morning and afternoon on one day during summer (August) and two days in winter (December and January). Their emission rates were determined and it was observed that during summer relatively higher amounts of the selected odorous compounds were emitted compared to winter. Air samples from primary settling basin, aeration basin, and final settling basin were tested and the total amount of selected odorous compounds emitted per wastewater ton was found to be 1344 ?g/m(3) from the selected treatment processes. It was also observed that, in this study, the dominant odor intensity contribution was caused by dimethyl disulfide (69.1%). PMID:22389601

  11. Emission Characteristics and Factors of Selected Odorous Compounds at a Wastewater Treatment Plant

    PubMed Central

    Jeon, Eui-Chan; Son, Hyun-Keun; Sa, Jae-Hwan

    2009-01-01

    This study was initiated to explore the emission characteristics of Reduced Sulfur Compounds (RSCs: hydrogen sulfide, methyl mercaptan, dimethyl sulfide, dimethyl disulfide), ammonia and trimethylamine from a Wastewater Treatment Plant (WWTP) located at Sun-Cheon, Chonlanam-Do in South Korea. The study also evaluates flux profiles of the six selected odorous compounds and their flux rates (?g/m2/min) and compares their emission characteristics. A Dynamic Flux Chamber DFC was used to measure fluxes of pollutants from the treatment plant. Quality control of odor samples using a non-reactive sulfur dioxide gas determined the time taken for DFC concentration to reach equilibrium. The reduced sulfur compounds were analyzed by interfacing gas chromatography with a Pulsed Flame Photometric Detector (PFPD). Air samples were collected in the morning and afternoon on one day during summer (August) and two days in winter (December and January). Their emission rates were determined and it was observed that during summer relatively higher amounts of the selected odorous compounds were emitted compared to winter. Air samples from primary settling basin, aeration basin, and final settling basin were tested and the total amount of selected odorous compounds emitted per wastewater ton was found to be 1344 ?g/m3 from the selected treatment processes. It was also observed that, in this study, the dominant odor intensity contribution was caused by dimethyl disulfide (69.1%). PMID:22389601

  12. Catalytic Destruction Of Toxic Organic Compounds

    NASA Technical Reports Server (NTRS)

    Voecks, Gerald E.

    1990-01-01

    Proposed process disposes of toxic organic compounds in contaminated soil or carbon beds safely and efficiently. Oxidizes toxic materials without producing such other contaminants as nitrogen oxides. Using air, fuel, catalysts, and steam, system consumes less fuel and energy than decontamination processes currently in use. Similar process regenerates carbon beds used in water-treatment plants.

  13. Global Exposure Modelling of Semivolatile Organic Compounds

    NASA Astrophysics Data System (ADS)

    Guglielmo, F.; Lammel, G.; Maier-Reimer, E.

    2008-12-01

    Organic compounds which are persistent and toxic as the agrochemicals ?-hexachlorocyclohexane (?-HCH, lindane) and dichlorodiphenyltrichloroethane (DDT) pose a hazard for the ecosystems. These compounds are semivolatile, hence multicompartmental substances and subject to long-range transport (LRT) in atmosphere and ocean. Being lipophilic, they accumulate in exposed organism tissues and biomagnify along food chains. The multicompartmental global fate and LRT of DDT and lindane in the atmosphere and ocean have been studied using application data for 1980, on a decadal scale using a model based on the coupling of atmosphere and (for the first time for these compounds) ocean General Circulation Models (ECHAM5 and MPI-OM). The model system encompasses furthermore 2D terrestrial compartments (soil and vegetation) and sea ice, a fully dynamic atmospheric aerosol (HAM) module and an ocean biogeochemistry module (HAMOCC5). Large mass fractions of the compounds are found in soil. Lindane is also found in comparable amount in ocean. DDT has the longest residence time in almost all compartments. The sea ice compartment locally almost inhibits volatilization from the sea. The air/sea exchange is also affected , up to a reduction of 35 % for DDT by partitioning to the organic phases (suspended and dissolved particulate matter) in the global oceans. Partitioning enhances vertical transport in the sea. Ocean dynamics are found to be more significant for vertical transport than sinking associated with particulate matter. LRT in the global environment is determined by the fast atmospheric circulation. Net meridional transport taking place in the ocean is locally effective mostly via western boundary currents, upon applications at mid- latitudes. The pathways of the long-lived semivolatile organic compounds studied include a sequence of several cycles of volatilisation, transport in the atmosphere, deposition and transport in the ocean (multihopping substances). Multihopping is more significant for DDT than for lindane. It enhances the LRT potential for both compounds.

  14. Compositing water samples for analysis of volatile organic compounds

    USGS Publications Warehouse

    Lopes, T.J.; Fallon, J.D.; Maluk, T.L.

    2000-01-01

    Accurate mean concentrations of volatile organic compounds (VOCs) can easily and economically be obtained from a single VOC analysis by using proven methods of collecting representative, discrete water samples and compositing them with a gas-tight syringe. The technique can be used in conjunction with chemical analysis by a conventional laboratory, field-portable equipment, or a mobile laboratory. The type of mean concentration desired depends on the objectives of monitoring. For example, flow-weighted mean VOC concentrations can be used to estimate mass loadings in wastewater and urban storm water, and spatially integrated mean VOC concentrations can be used to assess sources of drinking water (e.g., reservoirs and rivers). The mean error in a discrete sample due to compositing is about 2% for most VOC concentrations greater than 0.1 ??g/L. The total error depends on the number of discrete samples comprising the composite sample and precision of the chemical analysis.Accurate mean concentrations of volatile organic compounds (VOCs) can easily and economically be obtained from a single VOC analysis by using proven methods of collecting representative, discrete water samples and compositing them with a gas-tight syringe. The technique can be used in conjunction with chemical analysis by a conventional laboratory, field-portable equipment, or a mobile laboratory. The type of mean concentration desired depends on the objectives of monitoring. For example, flow-weighted mean VOC concentrations can be used to estimate mass loadings in wastewater and urban storm water, and spatially integrated mean VOC concentrations can be used to assess sources of drinking water (e.g., reservoirs and rivers). The mean error in a discrete sample due to compositing is about 2% for most VOC concentrations greater than 0.1 ??g/L. The total error depends on the number of discrete samples comprising the composite sample and precision of the chemical analysis.Researchers are able to derive accurate values for the mean concentration of VOCs from a single VOC analysis using established techniques for the collection of representative, discrete water samples. Such samples are then composited with a gas-tight syringe. This methodology can be employed in conjunction with chemical assessment using a conventional laboratory, field-portable equipment, or a mobile laboratory. Estimates of mass loadings in wastewater and urban storm runoff can be generated using values for the flow-weighted mean VOC concentrations. Spatially integrated mean VOC concentrations are useful for the evaluation of drinking waters. Factors that influence the value for the total error are identified.

  15. Urban contribution of pharmaceuticals and other organic wastewater contaminants to streams during differing flow conditions

    USGS Publications Warehouse

    Kolpin, D.W.; Skopec, M.; Meyer, M.T.; Furlong, E.T.; Zaugg, S.D.

    2004-01-01

    During 2001, 76 water samples were collected upstream and downstream of select towns and cities in Iowa during high-, normal- and low-flow conditions to determine the contribution of urban centers to concentrations of pharmaceuticals and other organic wastewater contaminants (OWCs) in streams under varying flow conditions. The towns ranged in population from approximately 2000 to 200000. Overall, one or more OWCs were detected in 98.7% of the samples collected, with 62 of the 105 compounds being found. The most frequently detected compounds were metolachlor (pesticide), cholesterol (plant and animal sterol), caffeine (stimulant), ??-sitosterol (plant sterol) and 1,7-dimethylxanthine (caffeine degradate). The number of OWCs detected decreased as streamflow increased from low- (51 compounds detected) to normal- (28) to high-flow (24) conditions. Antibiotics and other prescription drugs were only frequently detected during low-flow conditions. During low-flow conditions, 15 compounds (out of the 23) and ten compound groups (out of 11) detected in more than 10% of the streams sampled had significantly greater concentrations in samples collected downstream than in those collected upstream of the urban centers. Conversely, no significant differences in the concentrations were found during high-flow conditions. Thus, the urban contribution of OWCs to streams became progressively muted as streamflow increased. ?? 2004 Elsevier B.V. All rights reserved.

  16. Strategies to characterize polar organic contamination in wastewater: exploring the capability of high resolution mass spectrometry.

    PubMed

    Schymanski, Emma L; Singer, Heinz P; Longrée, Philipp; Loos, Martin; Ruff, Matthias; Stravs, Michael A; Ripollés Vidal, Cristina; Hollender, Juliane

    2014-01-01

    Wastewater effluents contain a multitude of organic contaminants and transformation products, which cannot be captured by target analysis alone. High accuracy, high resolution mass spectrometric data were explored with novel untargeted data processing approaches (enviMass, nontarget, and RMassBank) to complement an extensive target analysis in initial "all in one" measurements. On average 1.2% of the detected peaks from 10 Swiss wastewater treatment plant samples were assigned to target compounds, with 376 reference standards available. Corrosion inhibitors, artificial sweeteners, and pharmaceuticals exhibited the highest concentrations. After blank and noise subtraction, 70% of the peaks remained and were grouped into components; 20% of these components had adduct and/or isotope information available. An intensity-based prioritization revealed that only 4 targets were among the top 30 most intense peaks (negative mode), while 15 of these peaks contained sulfur. Of the 26 nontarget peaks, 7 were tentatively identified via suspect screening for sulfur-containing surfactants and one peak was identified and confirmed as 1,3-benzothiazole-2-sulfonate, an oxidation product of a vulcanization accelerator. High accuracy, high resolution data combined with tailor-made nontarget processing methods (all available online) provided vital information for the identification of a wider range of heteroatom-containing compounds in the environment. PMID:24417318

  17. Nonvolatile organic compounds in treated waters.

    PubMed Central

    Watts, C D; Crathorne, B; Fielding, M; Killops, S D

    1982-01-01

    Over the past decade much information has been published on the analysis of organics extracted from treated water. Certain of these organics have been shown to be by-products of the chlorination disinfection process and to possess harmful effects at high concentrations. This has resulted in increased interest in alternative disinfection processes, particularly ozonation. The data on organics had been largely obtained by using gas chromatography-mass spectrometry, which is only capable of analyzing, at best, 20% of the organics present in treated water. Research in key areas such as mutagenicity testing of water and characterization of chlorination and ozonation by-products has emphasized the need for techniques suitable for analysis of the remaining nonvolatile organics. Several methods for the isolation of nonvolatile organics have been evaluated and, of these, freeze-drying followed by methanol extraction appears the most suitable. Reverse-phase HPLC was used for separation of the methanol extract, but increased resolution for separation of the complex mixtures present is desirable. In this context, high resolution size exclusion chromatography shows promise. Characterization of separated nonvolatiles is possible by the application of state-of-the-art mass spectrometric techniques. Results obtained by these techniques have shown that the nonvolatile organic fraction of chlorinated drinking water consists of many discrete compounds. Among these, some of the chlorinated compounds are almost certainly by-products of disinfection. Studies of the by-products of ozonation of fulvic and humic acids isolated from river waters have indicated a similar proportion of nonvolatile organics. Further, ozonation can result in the release of compounds that are trapped in the macromolecules. PMID:6759110

  18. 40 CFR Table 34 to Subpart G of... - Fraction Measured (Fm) and Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...Fm ) and Fraction Emitted (Fe ) For HAP Compounds in Wastewater Streams Chemical name CAS...Service registry number assigned to specific compounds, isomers, or mixtures of compounds. [59 FR 19468, Apr. 22, 1994, as...

  19. Organic photosensitive devices using subphthalocyanine compounds

    DOEpatents

    Rand, Barry (Princeton, NJ); Forrest, Stephen R. (Ann Arbor, MI); Mutolo, Kristin L. (Hollywood, CA); Mayo, Elizabeth (Alhambra, CA); Thompson, Mark E. (Anaheim Hills, CA)

    2011-07-05

    An organic photosensitive optoelectronic device, having a donor-acceptor heterojunction of a donor-like material and an acceptor-like material and methods of making such devices is provided. At least one of the donor-like material and the acceptor-like material includes a subphthalocyanine, a subporphyrin, and/or a subporphyrazine compound; and/or the device optionally has at least one of a blocking layer or a charge transport layer, where the blocking layer and/or the charge transport layer includes a subphthalocyanine, a subporphyrin, and/or a subporphyrazine compound.

  20. Toxic organic compounds from energy production

    SciTech Connect

    Hites, R.A.

    1991-09-20

    The US Department of Energy's Office of Health and Environmental Research (OHER) has supported work in our laboratory since 1977. The general theme of this program has been the identification of potentially toxic organic compounds associated with various combustion effluents, following the fates of these compounds in the environment, and improving the analytical methodology for making these measurements. The projects currently investigation include: an improved sampler for semi-volatile compounds in the atmosphere; the wet and dry deposition of dioxins and furans from the atmosphere; the photodegradation and mobile sources of dioxins and furans; and the bioaccumulation of PAH by tree bark. These projects are all responsive to OHER's interest in the pathways and mechanisms by which energy-related agents move through and are modified by the atmosphere''. The projects on gas chromatographic and liquid chromatographic tandem mass spectrometry are both responsive to OHER's interest in new and more sensitive technologies for chemical measurements''. 35 refs., 9 figs.

  1. 40 CFR Table 8 to Subpart G of... - Organic HAP's Subject to the Wastewater Provisions for Process Units at New Sources

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...false Organic HAP's Subject to the Wastewater Provisions for Process Units at New...Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 8 Table...63—Organic HAP's Subject to the Wastewater Provisions for Process Units at...

  2. 40 CFR Table 9 to Subpart G of... - Organic HAP's Subject to the Wastewater Provisions for Process Units at New and Existing Sources...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...false Organic HAP's Subject to the Wastewater Provisions for Process Units at New...Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 9 Table...63—Organic HAP's Subject to the Wastewater Provisions for Process Units at...

  3. 40 CFR Table 8 to Subpart G of... - Organic HAP's Subject to the Wastewater Provisions for Process Units at New Sources

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...false Organic HAP's Subject to the Wastewater Provisions for Process Units at New...Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 8 Table...63—Organic HAP's Subject to the Wastewater Provisions for Process Units at...

  4. 40 CFR Table 9 to Subpart G of... - Organic HAP's Subject to the Wastewater Provisions for Process Units at New and Existing Sources...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...false Organic HAP's Subject to the Wastewater Provisions for Process Units at New...Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 9 Table...63—Organic HAP's Subject to the Wastewater Provisions for Process Units at...

  5. 40 CFR Table 9 to Subpart G of... - Organic HAP's Subject to the Wastewater Provisions for Process Units at New and Existing Sources...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...false Organic HAP's Subject to the Wastewater Provisions for Process Units at New...Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 9 Table...63—Organic HAP's Subject to the Wastewater Provisions for Process Units at...

  6. 40 CFR Table 8 to Subpart G of... - Organic HAP's Subject to the Wastewater Provisions for Process Units at New Sources

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...false Organic HAP's Subject to the Wastewater Provisions for Process Units at New...Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 8 Table...63—Organic HAP's Subject to the Wastewater Provisions for Process Units at...

  7. 40 CFR Table 9 to Subpart G of... - Organic HAP's Subject to the Wastewater Provisions for Process Units at New and Existing Sources...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...false Organic HAP's Subject to the Wastewater Provisions for Process Units at New...Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 9 Table...63—Organic HAP's Subject to the Wastewater Provisions for Process Units at...

  8. 40 CFR Table 8 to Subpart G of... - Organic HAP's Subject to the Wastewater Provisions for Process Units at New Sources

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...false Organic HAP's Subject to the Wastewater Provisions for Process Units at New...Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 8 Table...63—Organic HAP's Subject to the Wastewater Provisions for Process Units at...

  9. 40 CFR Table 8 to Subpart G of... - Organic HAP's Subject to the Wastewater Provisions for Process Units at New Sources

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...false Organic HAP's Subject to the Wastewater Provisions for Process Units at New...Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 8 Table...63—Organic HAP's Subject to the Wastewater Provisions for Process Units at...

  10. 40 CFR Table 9 to Subpart G of... - Organic HAP's Subject to the Wastewater Provisions for Process Units at New and Existing Sources...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...false Organic HAP's Subject to the Wastewater Provisions for Process Units at New...Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 9 Table...63—Organic HAP's Subject to the Wastewater Provisions for Process Units at...

  11. Potential toxic effects of aircraft de-icers and wastewater samples containing these compounds.

    PubMed

    Mohiley, A; Franzaring, J; Calvo, O C; Fangmeier, A

    2015-09-01

    One of the major problems of airport operation is the impact of pollution caused by runoff waters. Runoff waters at an airport may contain high concentrations of different contaminants resulting from various activities of its operation. High quantities of aircraft de-icing/anti-icing fluids are used annually at airports worldwide. Aircraft de-icers and anti-icers may have negative environmental impacts, but their effects on aquatic organisms are virtually unknown. In order to address this issue, aircraft de-icers, pavement de-icers and wastewater samples were obtained from a regional airport. To evaluate the toxicity of wastewater samples and aircraft de-icing/anti-icing fluids (ADAFs), two bio-tests were performed: the Lemna growth inhibition test according to OECD guideline 221 and the luminescent bacteria test according to ISO guideline 11348-2. In the Lemna growth inhibition test, phytotoxicity was assessed using the endpoints frond number and frond area. The luminescent bacteria test involved the marine bacterium Vibrio fischeri. The estimates of effective concentrations (EC50) values were determined using the free software R and the "drc" library. Aquatic plants and marine bacteria showed a higher sensitivity towards ADAFs than to wastewater samples. Experiments showed that aircraft de-icing/anti-icing fluids and wastewater samples were relatively more toxic towards Lemna gibba L. in comparison to V. fischeri. PMID:25925142

  12. Organic compounds in star forming regions.

    PubMed

    Kochina, O; Wiebe, D

    2014-09-01

    The influence of complex dust composition on the general chemical evolution of a prestellar core and the content of complex organic compounds is studied. It is shown that various component groups respond differently to the presence of a small dust population. At early stages the difference is determined primarily by changes in the balance of photo processes due to effective absorption of ultraviolet photons by small dust grains of the second population and collisional reactions with dust particles. At later stages differences are also caused by the growing dominance of additional reaction channels related to surface organic synthesis. PMID:25515345

  13. Microbiological degradation of atmospheric organic compounds

    NASA Astrophysics Data System (ADS)

    Ariya, Parisa A.; Nepotchatykh, Oleg; Ignatova, Olga; Amyot, Marc

    2002-11-01

    Until now, aerosol transformation was assumed to be via chemical or physical processes. Here we present evidence that an important class of organic aerosols - dicarboxylic acids (DCA) - can be efficiently transformed by existing airborne microbes (bacteria and fungi) in the boundary layer. Isotopic studies indicate that microbiological entities transform and use DCA as nutrients. Several observed products are toxicants or pathogens. Identified volatile products indicate that DCA can be recycled back to the atmosphere via microbiological processes. Thus, biodegradation could be an important atmospheric transformation pathway for organic compounds.

  14. Metabolic Reactions among Organic Sulfur Compounds

    NASA Technical Reports Server (NTRS)

    Schulte, M.; Rogers, K.

    2005-01-01

    Sulfur is central to the metabolisms of many organisms that inhabit extreme environments. Numerous authors have addressed the energy available from a variety of inorganic sulfur redox pairs. Less attention has been paid, however, to the energy required or gained from metabolic reactions among organic sulfur compounds. Work in this area has focused on the oxidation of alkyl sulfide or disulfide to thiol and formaldehyde, e.g. (CH3)2S + H2O yields CH3SH + HCHO + H2, eventually resulting in the formation of CO2 and SO4(-2). It is also found that reactions among thiols and disulfides may help control redox disequilibria between the cytoplasm and the periplasm. Building on our earlier efforts for thiols, we have compiled and estimated thermodynamic properties for alkyl sulfides. We are investigating metabolic reactions among various sulfur compounds in a variety of extreme environments, ranging from sea floor hydrothermal systems to organic-rich sludge. Using thermodynamic data and the revised HKF equation of state, along with constraints imposed by the geochemical environments sulfur-metabolizing organisms inhabit, we are able to calculate the amount of energy available to these organisms.

  15. Occurrence and Implication of dissolved organic phosphorus (DOP) in tertiary wastewater Effluents Page 1 of 6

    E-print Network

    Chen, Zhongping

    GU, APRIL Occurrence and Implication of dissolved organic phosphorus (DOP) in tertiary wastewater wastewater effluents L. Liu1 , D. S. Smith2 , M. Bracken3 , J.B. Neethling4 , H.D. Stensel5 and S. Murthy6 levels (e.g. TPwastewater treatment plants. A few previous studies (Benisch et al., 2007

  16. Simultaneous removal of perchlorate and energetic compounds in munitions wastewater by zero-valent iron and perchlorate-respiring bacteria.

    PubMed

    Ahn, Se Chang; Hubbard, Brian; Cha, Daniel K; Kim, Byung J

    2014-01-01

    Ammonium perchlorate is one of the main constituents in Army's insensitive melt-pour explosive, PAX-21 in addition to RDX and 2,4-dinitroanisole (DNAN). The objective of this study is to develop an innovative treatment process to remove both perchlorate and energetic compounds simultaneously from PAX-21 production wastewater. It was hypothesized that the pretreatment of PAX-21 wastewater with zero-valent iron (ZVI) would convert energetic compounds to products that are more amenable for biological oxidation and that these products serve as electron donors for perchlorate-reducing bacteria. Results of batch ZVI reduction experiments showed that DNAN was completely reduced to 2,4-diaminoanisole and RDX was completely reduced to formaldehyde. Anaerobic batch biodegradation experiments showed that perchlorate (30 mg L(-1)) in ZVI-treated PAX-21 wastewater was decreased to an undetectable level after 5 days. Batch biodegradation experiments also confirmed that formaldehyde in ZVI-treated wastewater was the primary electron donor for perchlorate-respiring bacteria. The integrated iron-anaerobic bioreactor system was effective in completely removing energetic compounds and perchlorate from the PAX-21 wastewater without adding an exogenous electron donor. This study demonstrated that ZVI pretreatment not only removed energetic compounds, but also transformed energetic compounds to products that can serve as the source of electrons for perchlorate-respiring bacteria. PMID:24410688

  17. Self assembly properties of primitive organic compounds

    NASA Technical Reports Server (NTRS)

    Deamer, D. W.

    1991-01-01

    A central event in the origin of life was the self-assembly of amphiphilic, lipid-like compounds into closed microenvironments. If a primitive macromolecular replicating system could be encapsulated within a vesicular membrane, the components of the system would share the same microenvironment, and the result would be a step toward true cellular function. The goal of our research has been to determine what amphiphilic molecules might plausibly have been available on the early Earth to participate in the formation of such boundary structures. To this end, we have investigated primitive organic mixtures present in carbonaceous meteorites such as the Murchison meteorite, which contains 1-2 percent of its mass in the form of organic carbon compounds. It is likely that such compounds contributed to the inventory of organic carbon on the prebiotic earth, and were available to participate in chemical evolution leading to the emergence of the first cellular life forms. We found that Murchison components extracted into non-polar solvent systems are surface active, a clear indication of amphiphilic character. One acidic fraction self-assembles into vesicular membranes that provide permeability barriers to polar solutes. Other evidence indicates that the membranes are bimolecular layers similar to those formed by contemporary membrane lipids. We conclude that bilayer membrane formation by primitive amphiphiles on the early Earth is feasible. However, only a minor fraction of acidic amphiphiles assembles into bilayers, and the resulting membranes require narrowly defined conditions of pH and ionic composition to be stable. It seems unlikely, therefore, that meteoritic infall was a direct source of membrane amphiphiles. Instead, the hydrocarbon components and their derivatives more probably would provide an organic stock available for chemical evolution. Our current research is directed at possible reactions which would generate substantial quantities of membranogenic amphiphiles. One possibility is photochemical oxidation of hydrocarbons.

  18. Polyphenolic compounds progress during olive mill wastewater sludge and poultry manure co-composting, and humic substances building (Southeastern Tunisia).

    PubMed

    Rigane, Hafedh; Chtourou, Mohamed; Ben Mahmoud, Imen; Medhioub, Khaled; Ammar, Emna

    2015-01-01

    In Mediterranean areas, olive mill wastes pose a major environmental problem owing to their important production and their high polyphenolic compounds and organic acids concentrations. In this work, the evolution of polyphenolic compounds was studied during co-composting of olive mill wastewater sludge and poultry manure, based on qualitative (G-50 sephadex) and quantitative (Folin-Ciocalteu), as well as high pressure liquid chromatography analyses. Results showed a significant polyphenolic content decrease of 99% and a noticeable transformation of low to high molecular weight fraction during the compost maturation period. During this step, polyphenols disappearance suggested their assimilation by thermophilic bacteria as a carbon and energy source, and contributed to humic substances synthesis. Polyphenolic compounds, identified initially by high pressure liquid chromatography, disappeared by composting and only traces of caffeic, coumaric and ferulic acids were detected in the compost. In the soil, the produced compost application improved the chemical and physico-chemical soil properties, mainly fertilising elements such as calcium, magnesium, nitrogen, potassium and phosphorus. Consequently, a higher potato production was harvested in comparison with manure amendment. PMID:25502693

  19. 40 CFR 60.462 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 2011-07-01 false Standards for volatile organic compounds. 60.462 Section 60.462 Protection...Surface Coating § 60.462 Standards for volatile organic compounds. (a) On and after the date on...

  20. 40 CFR 60.712 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 2011-07-01 false Standards for volatile organic compounds. 60.712 Section 60.712 Protection...Coating Facilities § 60.712 Standards for volatile organic compounds. Each owner or operator of any...

  1. 40 CFR 60.742 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 2011-07-01 false Standards for volatile organic compounds. 60.742 Section 60.742 Protection...Substrates Facilities § 60.742 Standards for volatile organic compounds. (a) Each owner or operator of...

  2. Palladium catalyzed hydrogenation of bio-oils and organic compounds

    DOEpatents

    Elliott, Douglas C [Kennewick, WA; Hu, Jianli [Richland, WA; Hart,; Todd, R [Kennewick, WA; Neuenschwander, Gary G [Burbank, WA

    2011-06-07

    The invention provides palladium-catalyzed hydrogenations of bio-oils and certain organic compounds. Experimental results have shown unexpected and superior results for palladium-catalyzed hydrogenations of organic compounds typically found in bio-oils.

  3. Palladium catalyzed hydrogenation of bio-oils and organic compounds

    DOEpatents

    Elliott, Douglas C. (Richland, WA); Hu, Jianli (Kennewick, WA); Hart, Todd R. (Kennewick, WA); Neuenschwander, Gary G. (Burbank, WA)

    2008-09-16

    The invention provides palladium-catalyzed hydrogenations of bio-oils and certain organic compounds. Experimental results have shown unexpected and superior results for palladium-catalyzed hydrogenations of organic compounds typically found in bio-oils.

  4. 40 CFR 60.392 - Standards for volatile organic compounds

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 2010-07-01 false Standards for volatile organic compounds 60.392 Section 60.392 Protection of Environment...Coating Operations § 60.392 Standards for volatile organic compounds On and after the date on which the initial...

  5. 40 CFR 60.712 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 2010-07-01 false Standards for volatile organic compounds. 60.712 Section 60.712 Protection of Environment...Coating Facilities § 60.712 Standards for volatile organic compounds. Each owner or operator of any affected...

  6. 40 CFR 60.492 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 2010-07-01 false Standards for volatile organic compounds. 60.492 Section 60.492 Protection of Environment...Coating Industry § 60.492 Standards for volatile organic compounds. On or after the date on which the initial...

  7. 40 CFR 60.742 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 2010-07-01 false Standards for volatile organic compounds. 60.742 Section 60.742 Protection of Environment...Substrates Facilities § 60.742 Standards for volatile organic compounds. (a) Each owner or operator of an affected...

  8. 40 CFR 60.622 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 2010-07-01 false Standards for volatile organic compounds. 60.622 Section 60.622 Protection of Environment...Dry Cleaners § 60.622 Standards for volatile organic compounds. (a) Each affected petroleum solvent dry...

  9. Fractionation and characterization of organic matter in wastewater from a swine waste-retention basin

    USGS Publications Warehouse

    Leenheer, Jerry A.; Rostad, Colleen E.

    2004-01-01

    Organic matter in wastewater sampled from a swine waste-retention basin in Iowa was fractionated into 14 fractions on the basis of size (particulate, colloid, and dissolved); volatility; polarity (hydrophobic, transphilic, hydrophilic); acid, base, neutral characteristics; and precipitate or flocculates (floc) formation upon acidification. The compound-class composition of each of these fractions was determined by infrared and 13C-NMR spectral analyses. Volatile acids were the largest fraction with acetic acid being the major component of this fraction. The second most abundant fraction was fine particulate organic matter that consisted of bacterial cells that were subfractionated into extractable lipids consisting of straight chain fatty acids, peptidoglycans components of bacterial cell walls, and protein globulin components of cellular plasma. The large lipid content of the particulate fraction indicates that non-polar contaminants, such as certain pharmaceuticals added to swine feed, likely associate with the particulate fraction through partitioning interactions. Hydrocinnamic acid is a major component of the hydrophobic acid fraction, and its presence is an indication of anaerobic degradation of lignin originally present in swine feed. This is the first study to combine particulate organic matter with dissolved organic matter fractionation into a total organic matter fractionation and characterization.

  10. A national reconnaissance of pharmaceuticals and other organic wastewater contaminants in the United States - I) Groundwater

    USGS Publications Warehouse

    Barnes, K.K.; Kolpin, D.W.; Furlong, E.T.; Zaugg, S.D.; Meyer, M.T.; Barber, L.B.

    2008-01-01

    As part of the continuing effort to collect baseline information on the environmental occurrence of pharmaceuticals, and other organic wastewater contaminants (OWCs) in the Nation's water resources, water samples were collected from a network of 47 groundwater sites across 18 states in 2000. All samples collected were analyzed for 65 OWCs representing a wide variety of uses and origins. Site selection focused on areas suspected to be susceptible to contamination from either animal or human wastewaters (i.e. down gradient of a landfill, unsewered residential development, or animal feedlot). Thus, sites sampled were not necessarily used as a source of drinking water but provide a variety of geohydrologic environments with potential sources of OWCs. OWCs were detected in 81% of the sites sampled, with 35 of the 65 OWCs being found at least once. The most frequently detected compounds include N,N-diethyltoluamide (35%, insect repellant), bisphenol A (30%, plasticizer), tri(2-chloroethyl) phosphate (30%, fire retardant), sulfamethoxazole (23%, veterinary and human antibiotic), and 4-octylphenol monoethoxylate (19%, detergent metabolite). Although sampling procedures were intended to ensure that all groundwater samples analyzed were indicative of aquifer conditions it is possible that detections of some OWCs could have resulted from leaching of well-construction materials and/or other site-specific conditions related to well construction and materials. Future research will be needed to identify those factors that are most important in determining the occurrence and concentrations of OWCs in groundwater.

  11. Impact of treated wastewater on organismic biosensors at various levels of biological organization.

    PubMed

    Topi? Popovi?, Natalija; Strunjak-Perovi?, Ivan?ica; Klobu?ar, Roberta Sauerborn; Bariši?, Josip; Babi?, Sanja; Jadan, Margita; Kepec, Slavko; Kazazi?, Snježana P; Matijatko, Vesna; Beer Ljubi?, Blanka; Car, Ivan; Repec, Siniša; Stipani?ev, Draženka; Klobu?ar, Goran I V; ?ož-Rakovac, Rozelindra

    2015-12-15

    Relating the treated wastewater quality and its impact on organismic biosensors (Prussian carp, Carassius gibelio and earthworm, Eisenia fetida) was the main objective of the study. The impact on health status of fish living downstream, microbiological contamination and antimicrobial resistance, fish tissue structure, blood biochemistry, oxidative stress, genotoxic effects, as well as multixenobiotic resistance mechanism (MXR) was assessed. Treated wastewater discharged from the WWTP modified the environmental parameters and xenobiotic concentrations of the receiving surface waters. Potential bacterial pathogens from fish and respective waters were found in relatively low numbers, although they comprised aeromonads with a zoonotic potential. High resistance profiles were determined towards the tested antimicrobial compounds, mostly sulfamethoxazole and erythromycin. Histopathology primarily revealed gill lamellar fusion and reduction of interlamellar spaces of effluent fish. A significant increase in plasma values of urea, total proteins, albumins and triglycerides and a significant decrease in the activity of plasma superoxide dismutase were noted in carp from the effluent-receiving canal. Micronucleus test did not reveal significant differences between the examined groups, but a higher frequency of erythrocyte nuclear abnormalities was found in fish sampled from the effluent-receiving canal. Earthworms indicated to the presence of MXR inhibitors in water and sludge samples, thus proving as a sensitive sentinel organism for environmental pollutants. The integrative approach of this study could serve as a guiding principle in conducting evaluations of the aquatic habitat health in complex bio-monitoring studies. PMID:26298246

  12. [Source profile of volatile carbonyl compounds in wastewater treatment plant of an oil refinery].

    PubMed

    Zhou, Bo-Yu; Liu, Wang; Wang, Bo-Guang; Zhou, Mi; Huang, Qing; Zhou, Lei

    2013-07-01

    An observation was conducted at the wastewater treatment plant in a refinery in Guangdong province, using the PFPH-GC/MS method to analyze the composition and the concentration of volatile carbonyl compounds. The emission characteristics and the atmospheric chemical reactivity of these compounds were also studied. The results showed that 20 kinds of carbonyl compounds were detected with a concentration range of 0 to 68.80 microg x m(-3). The mean value of total concentration in all processing unit was (253.02 +/- 124.5) microg x m(-3). Background corrected concentrations showed that for each of the 6 treatment units of the plant, over 90% of the volatile carbonyl emissions were contributed by 14 of the 20 volatile carbonyl compounds, among which aldehyde was the most abundant with an average concentration of (44.74 +/- 20.89) microg x m(-3), followed by 2-butanone and acetaldehyde with average concentrations of (30.47 +/- 12.94) microg x m(-3) and (23.51 +/- 14.57) microg x m(-3), respectively. Several molecular markers were identified based on the analysis of the chemical activities and atmospheric lifetimes of the 20 carbonyl compounds. Finally, a source profile was established for the plant. PMID:24027983

  13. Biogenic volatile organic compounds - small is beautiful

    NASA Astrophysics Data System (ADS)

    Owen, S. M.; Asensio, D.; Li, Q.; Penuelas, J.

    2012-12-01

    While canopy and regional scale flux measurements of biogenic volatile organic compounds (bVOCs) are essential to obtain an integrated picture of total compound reaching the atmosphere, many fascinating and important emission details are waiting to be discovered at smaller scales, in different ecological and functional compartments. We concentrate on bVOCs below ground to <2m above ground level. Emissions at leaf scale are well documented and widely presented, and are not discussed here. Instead we describe some details of recent research on rhizosphere bVOCs, and bVOCs associated with pollination of flowers. Although bVOC emissions from soil surfaces are small, bVOCs are exuded by roots of some plant species, and can be extracted from decaying litter. Naturally occurring monoterpenes in the rhizosphere provide a specialised carbon source for micro-organisms, helping to define the micro-organism community structure, and impacting on nutrient cycles which are partly controlled by microorganisms. Naturally occurring monoterpenes in the soil system could also affect the aboveground structure of ecosystems because of their role in plant defence strategies and as mediating chemicals in allelopathy. A gradient of monoterpene concentration was found in soil around Pinus sylvestris and Pinus halepensis, decreasing with distance from the tree. Some compounds (?-pinene, sabinene, humulene and caryophyllene) in mineral soil were linearly correlated with the total amount of each compound in the overlying litter, indicating that litter might be the dominant source of these compounds. However, ?-pinene did not fall within the correlation, indicating a source other than litter, probably root exudates. We also show that rhizosphere bVOCs can be a carbon source for soil microbes. In a horizontal gradient from Populus tremula trees, microbes closest to the tree trunk were better enzymatically equipped to metabolise labeled monoterpene substrate. Monoterpenes can also increase the degradation rate in soil of the persistant organic pollutants, likely acting as analogues for the cometabo-lism of polychlorinated biphenyls (PCBs) Flowers of a ginger species (Alpinia kwangsiensis) and a fig species (Ficus hispida) showed different bVOC signals pre- and post pollination. For Ficus hispida, there are three floral stages of a fig-wasp dependency mechanism: receptive, post pollinator and interfloral. Of 28 compounds detected, transcaryophyllene with trans-?-farnesene were the most important at the receptor stage, trans-caryophyllene was the most abundant at the post-pollinator stage, and isoprene was the most abundant in the interfloral stage. Alpinia kwangsiensis presents two morphologies for the reproductive parts of the flower. The "anaflexistyle" morphology has the flower style lowered in the morning and raised in the afternoon. This is reversed for the "cataflexistyle" morphology. The bVOC mixture emitted by each morphology in morning and afternoon was complex. However for compounds showing a difference (cis-ocimene and Z + E epoxy -ocimene), the emissions from the anaflexistyle were greater than from the cataflexistyle, and were greater in the afternoon compared with the morning emissions. Where large flowering plant species are abundant, big changes in monoterpene emissions at < 2m above ground level over relatively small periods of time during pollination are likely to be missed in larger scale integrated flux measurements.

  14. DENSITY LEVELS OF PATHOGENIC ORGANISMS IN MUNICIPAL WASTEWATER SLUDGE: A LITERATURE REVIEW

    EPA Science Inventory

    This report presents a critical review of the literature from laboratory and full scale studies regarding density levels of indicator and pathogenic organisms in municipal wastewater sludges and septage. The effectiveness of conventional municipal sludge stabilization processes (...

  15. DISTRIBUTION OF ORGANIC WASTEWATER CONTAMINANTS BETWEEN WATER AND SEDIMENT IN SURFACE WATERS OF THE UNITED STATES

    EPA Science Inventory

    Trace concentrations of pharmaceuticals and other organic wastewater contaminants have been determined in the surface waters of Europe and the United States. A preliminary report of substantially higher concentrations of pharmaceuticals in sediment suggests that bottom sediment ...

  16. A review of organic UV-filters in wastewater treatment plants.

    PubMed

    Ramos, Sara; Homem, Vera; Alves, Arminda; Santos, Lúcia

    2016-01-01

    UV-filters are a group of compounds which have been massively used in the past years due to the recent concerns with sunburns, premature skin ageing and the risk of developing skin cancer, related to sun exposure. At the moment, these compounds have been identified by the scientific community as emerging pollutants, due to their persistence in the environment, potential to accumulate in biota and potential threat as endocrine disruptors. At some point, the majority of sunscreens will find their way into wastewater (due to bathing and washing activities) and because wastewater treatment plants (WWTPs) are not able to remove and/or degrade them, consequently they find their way into rivers, lakes and ocean, so it is not surprising that UV-filters are found in the environment. Therefore, wastewater treatment plants should be the focus of the scientific community aiming to better understand the fate of the UV-filters and develop new technologies to remove them from wastewater and sludge. This review, aims to provide the current state of the art in the occurrence and fate of UV-filters in wastewater treatment plants and how the technologies that are being used are successfully removing these compounds from both wastewater and sludge. PMID:26479831

  17. Water-Quality Data for Pharmaceuticals and Other Organic Wastewater Contaminants in Ground Water and in Untreated Drinking Water Sources in the United States, 2000-01

    USGS Publications Warehouse

    Barnes, Kimberlee K.; Kolpin, Dana W.; Focazio, Michael J.; Furlong, Edward T.; Meyer, Michael T.; Zaugg, Steven D.; Haack, Sheridan K.; Barber, Larry B.; Thurman, E. Michael

    2008-01-01

    This report presents water-quality data from two nationwide studies on the occurrence and distribution of organic wastewater contaminants. These data are part of the continuing effort of the U.S. Geological Survey Toxic Substances Hydrology Program to collect baseline information on the environmental occurrence of pharmaceuticals and other organic wastewater contaminants. In 2000, samples were collected from 47 ambient ground-water sites (not drinking-water wells) in 18 states and analyzed for 65 organic wastewater contaminants. In the summer of 2001, samples were collected from 74 sources of raw, untreated, drinking water in 25 states and Puerto Rico and analyzed for 100 organic wastewater contaminants. These sources comprise 25 ground-water and 49 surface-water sources of drinking water serving populations ranging from one family to more than 8 million people. Site selection for both studies focused on areas known or suspected to contain sources of animal and/or human wastewater. The five most frequently detected compounds in samples collected from ambient ground-water sites are N,N-diethyltoluamide (35 percent, insect repellant), bisphenol A (30 percent, plasticizer), tri(2-chloroethy) phosphate (30 percent, fire retardant), sulfamethoxazole (23 percent, veterinary and human antibiotic), and 4-octylphenol monoethoxylate (19 percent, detergent metabolite). The five most frequently detected organic wastewater contaminants in samples of untreated drinking water from surface-water sources are cholesterol (59 percent, natural sterol), metolachlor (53 percent, herbicide), cotinine (51 percent, nicotine metabolite), B -sitosterol (37 percent, natural plant sterol), and 1,7-dimethylxanthine (27 percent, caffeine metabolite). The five most frequently detected organic wastewater contaminants in samples of untreated drinking water from ground-water sources are tetrachloroethylene (24 percent, solvent), carbamazepine (20 percent, pharmaceutical), bisphenol A (20 percent, plasticizer), 1,7-dimethylxanthine (16 percent, caffeine metabolite), and tri(2-chloroethyl) phosphate (12 percent, fire retardant).

  18. Measurement of volatile organic compounds inside automobiles.

    PubMed

    Fedoruk, Marion J; Kerger, Brent D

    2003-01-01

    The objective of the current study was to evaluate the types and concentrations of volatile organic compounds (VOCs) in the passenger cabin of selected sedan automobiles under static (parked, unventilated) and specified conditions of operation (i.e., driving the vehicle using air conditioning alone, vent mode alone, or driver's window half open). Data were collected on five different passenger sedan vehicles from three major automobile manufacturers. Airborne concentrations were assessed using 90-min time-weighted average (TWA) samples under U.S. Environmental Protection Agency (USEPA) Method IP-1B to assess individual VOC compounds and total VOCs (TVOCs) calibrated to toluene. Static vehicle testing demonstrated TVOC levels of approximately 400-800 microg/m(3) at warm interior vehicle temperatures (approximately 80 degrees F), whereas TVOCs at least fivefold higher were observed under extreme heat conditions (e.g., up to 145 degrees F). The profile of most prevalent individual VOC compounds varied considerably according to vehicle brand, age, and interior temperature tested, with predominant compounds including styrene, toluene, and 8- to 12-carbon VOCs. TVOC levels under varied operating conditions (and ventilation) were generally four- to eightfold lower (at approximately 50-160 microg/m(3)) than the static vehicle measurements under warm conditions, with the lowest measured levels generally observed in the trials with the driver's window half open. These data indicate that while relatively high concentrations of certain VOCs can be measured inside static vehicles under extreme heat conditions, normal modes of operation rapidly reduce the inside-vehicle VOC concentrations even when the air conditioning is set on recirculation mode. PMID:12595882

  19. The influence of the buffering capacity on the production of organic acids and alcohols from wastewater in anaerobic reactor.

    PubMed

    Silva, A J; Pozzi, E; Foresti, E; Zaiat, M

    2015-02-01

    Some bacteria common in anaerobic digestion process can ferment a broad variety of organic compounds to organic acids, alcohols, and hydrogen, which can be used as biofuels. Researches are necessary to control the microbial interactions in favor of the alcohol production, as intermediary products of the anaerobic digestion of organic compounds. This paper reports on the effect of buffering capacity on the production of organic acids and alcohols from wastewater by a natural mixed bacterial culture. The hypothesis tested was that the increase of the buffering capacity by supplementation of sodium bicarbonate in the influent results in benefits for alcohol production by anaerobic fermentation of wastewater. When the influent was not supplemented with sodium bicarbonate, the chemical oxygen demand (COD)-ethanol and COD-methanol detected in the effluent corresponded to 22.5 and 12.7 % of the COD-sucrose consumed. Otherwise, when the reactor was fed with influent containing 0.5 g/L of sodium bicarbonate, the COD-ethanol and COD-methanol were effluents that corresponded to 39.2 and 29.6 % of the COD-sucrose consumed. Therefore, the alcohol production by supplementation of the influent with sodium bicarbonate was 33.6 % higher than the fermentation of the influent without sodium bicarbonate. PMID:25480346

  20. Identification of priority organic compounds in groundwater recharge of China.

    PubMed

    Li, Zhen; Li, Miao; Liu, Xiang; Ma, Yeping; Wu, Miaomiao

    2014-09-15

    Groundwater recharge using reclaimed water is considered a promising method to alleviate groundwater depletion, especially in arid areas. Traditional water treatment systems are inefficient to remove all the types of contaminants that would pose risks to groundwater, so it is crucial to establish a priority list of organic compounds (OCs) that deserve the preferential treatment. In this study, a comprehensive ranking system was developed to determine the list and then applied to China. 151 OCs, for which occurrence data in the wastewater treatment plants were available, were selected as candidate OCs. Based on their occurrence, exposure potential and ecological effects, two different rankings of OCs were established respectively for groundwater recharge by surface infiltration and direct aquifer injection. Thirty-four OCs were regarded as having no risks while the remaining 117 OCs were divided into three groups: high, moderate and low priority OCs. Regardless of the recharge way, nonylphenol, erythromycin and ibuprofen were the highest priority OCs; their removal should be prioritized. Also the database should be updated as detecting technology is developed. PMID:24960229

  1. A critical review on characterization strategies of organic matter for wastewater and water treatment processes.

    PubMed

    Tran, Ngoc Han; Ngo, Huu Hao; Urase, Taro; Gin, Karina Yew-Hoong

    2015-10-01

    The presence of organic matter (OM) in raw wastewater, treated wastewater effluents, and natural water samples has been known to cause many problems in wastewater treatment and water reclamation processes, such as treatability, membrane fouling, and the formation of potentially toxic by-products during wastewater treatment. This paper summarizes the current knowledge on the methods for characterization and quantification of OM in water samples in relation to wastewater and water treatment processes including: (i) characterization based on the biodegradability; (ii) characterization based on particle size distribution; (iii) fractionation based on the hydrophilic/hydrophobic properties; (iv) characterization based on the molecular weight (MW) size distribution; and (v) characterization based on fluorescence excitation emission matrix. In addition, the advantages, disadvantages and applications of these methods are discussed in detail. The establishment of correlations among biodegradability, hydrophobic/hydrophilic fractions, MW size distribution of OM, membrane fouling and formation of toxic by-products potential is highly recommended for further studies. PMID:26141666

  2. CHLORINATED ORGANIC COMPOUNDS IN DIGESTED, HEAT-CONDITIONED, AND PURIFAX-TREATED SLUDGES

    EPA Science Inventory

    Wastewater sludges were stabilized by Purifax treatment, anaerobic digestion and heat conditioning. The processed sludges from the Purifax process at chlorine dosages normally used in processing wastewater sludges contained 2 to > 14 times the total organic chlorine content of th...

  3. [Characterization of volatile organic compounds from indoor materials].

    PubMed

    Han, K; Jing, H

    1997-01-01

    Volatile organic compounds emitted from eight indoor materials including paint, wallpaper glue, maticolor coat, floorwax floor covering and air freshener and were analyzed by headspace GC-FID and GC-MS. About 3-30 organic compounds were detected from each material. It was shown that the emitted compounds and emission rate from different materials were different. The emitted compounds included paraffin, olefine, alcohol, aldehyde, ether, ester and aromatic compounds. The results of dynamic experiments in test chamber showed that the chamber concentration of volatile organic compounds from paint vs. time data follows a double exponent equation. PMID:15747466

  4. REDUCTION OF TOXICITY TO AQUATIC ORGANISMS BY INDUSTRIAL WASTEWATER TREATMENT

    EPA Science Inventory

    The specific goal of this research was to conduct 24-hour static acute bioassays with 'untreated' influent and 'treated' effluent using fathead minnows (Pimephales promelas) and water flea (Daphnia magna) to biologically evaluate the effectiveness of industrial wastewater facilit...

  5. Computational assessment of organic photovoltaic candidate compounds

    NASA Astrophysics Data System (ADS)

    Borunda, Mario; Dai, Shuo; Olivares-Amaya, Roberto; Amador-Bedolla, Carlos; Aspuru-Guzik, Alan

    2015-03-01

    Organic photovoltaic (OPV) cells are emerging as a possible renewable alternative to petroleum based resources and are needed to meet our growing demand for energy. Although not as efficient as silicon based cells, OPV cells have as an advantage that their manufacturing cost is potentially lower. The Harvard Clean Energy Project, using a cheminformatic approach of pattern recognition and machine learning strategies, has ranked a molecular library of more than 2.6 million candidate compounds based on their performance as possible OPV materials. Here, we present a ranking of the top 1000 molecules for use as photovoltaic materials based on their optical absorption properties obtained via time-dependent density functional theory. This computational search has revealed the molecular motifs shared by the set of most promising molecules.

  6. Ozone Production Potential of Volatile Organic Compounds

    NASA Astrophysics Data System (ADS)

    Butler, T.; Lawrence, M. G.; Lelieveld, J.

    2010-12-01

    Calculation of the ozone production potential of Volatile Organic Compounds (VOC) has traditionally been performed using so-called incremental reactivity techniques. Here were present a new approach to this problem using a photochemical box model with a tagged chemical mechanism. The results of our approach are consistent with previous work, but deliver much more detailed information about the VOC intermediate oxidation products involved in the production of ozone. We show that different classes of VOC exhibit very different temporal evolution in their modelled ozone production potential, with alkenes and reactive aromatic VOC producing ozone rapidly, while the ozone production potential of alkanes increases in the day after they are emitted. We suggest that this is related to the speed with which these different classes of compounds are able to produce very small oxidation fragments. We also relate the ozone production potential of VOC to the OH reactivity of the VOC oxidation intermediates, with indications that the oxidation products of alkenes and reactive aromatics are more efficient at producing ozone in their subsequent reactions with OH.

  7. Effects of treated wastewater irrigation on contents and dynamics of soil organic carbon and microbial activity

    NASA Astrophysics Data System (ADS)

    Jüschke, E.; Marschner, B.; Chen, Y.; Tarchitzky, J.

    2009-04-01

    In many arid and semi-arid regions, the demand for freshwater as drinking water and other domestic uses is constantly growing due to demographic growth and increasing standard of living. Therefore, less freshwater is available for agricultural irrigation and new water sources are needed. Treated wastewater (TWW) already serves as an important water source in Jordan, the Palestinian Territories and Israel. Related to its high loads with nutrients, salts and organic materials within its use as irrigation water major effects on the soil physical and chemical properties can occur, in the worst case leading to soil degradation. In an ongoing study we are investigated in the effects of TWW irrigation on agricultural soils in the region. Here we present results from analyses of total soil carbon contents and qualities in soils irrigated with freshwater and TWW. Furthermore microbiological parameters were investigated as microbial biomass, microbial activities and enzyme activities. In several sites, subsoils (50-160 cm) from TWW irrigated plots were depleted in soil organic matter with the largest differences occurring in sites with the longest TWW irrigation history. Laboratory incubation experiments with additions of 14C-labelled compounds to the soils showed that microbial activity in freshwater irrigated soils was much more stimulated by sugars or amino acids than in TWW irrigated soils. The lack of such "priming effects" (Hamer & Marschner 2005) in the TWW irrigated soils indicates that here the microorganisms are already operating at their optimal metabolic activity due to the continuous substrate inputs with soluble organic compounds from the TWW. Apparently, this higher microbial activity is causing an increased depletion of soil organic matter, which may have negative long-term effects on soil quality.

  8. Occurrence and fate of antibiotic, analgesic/anti-inflammatory, and antifungal compounds in five wastewater treatment processes.

    PubMed

    Guerra, P; Kim, M; Shah, A; Alaee, M; Smyth, S A

    2014-03-01

    The presence of pharmaceuticals and personal care products (PPCPs) in the aquatic environment as a result of wastewater effluent discharge is a concern in many countries. In order to expand our understanding on the occurrence and fate of PPCPs during wastewater treatment processes, 62 antibiotic, analgesic/anti-inflammatory, and antifungal compounds were analyzed in 72 liquid and 24 biosolid samples from six wastewater treatment plants (WWTPs) during the summer and winter seasons of 2010-2012. This is the first scientific study to compare five different wastewater treatment processes: facultative and aerated lagoons, chemically-enhanced primary treatment, secondary activated sludge, and advanced biological nutrient removal. PPCPs were detected in all WWTP influents at median concentrations of 1.5 to 92,000 ng/L, with no seasonal differences. PPCPs were also found in all final effluents at median levels ranging from 3.6 to 4,200 ng/L with higher values during winter (p<0.05). Removal efficiencies ranged between -450% and 120%, depending on the compound, WWTP type, and season. Mass balance showed that the fate of analgesic/anti-inflammatory compounds was predominantly biodegradation during biological treatment, while antibiotics and antifungal compounds were more likely to sorb to sludge. However, some PPCPs remained soluble and were detected in effluent samples. Overall, this study highlighted the occurrence and behavior of a large set of PPCPs and determined how their removal is affected by environmental/operational factors in different WWTPs. PMID:24370698

  9. 40 CFR Table 8 to Subpart Ggg of... - Fraction Measured (Fm) for HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 11 2011-07-01 2011-07-01 false Fraction Measured (Fm) for HAP Compounds in Wastewater Streams 8 Table 8 to Subpart GGG of Part 63 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES...

  10. 40 CFR Table 8 to Subpart Ggg of... - Fraction Measured (Fm) for HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 12 2013-07-01 2013-07-01 false Fraction Measured (Fm) for HAP Compounds in Wastewater Streams 8 Table 8 to Subpart GGG of Part 63 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES...

  11. 40 CFR Table 8 to Subpart Ggg of... - Fraction Measured (Fm) for HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 11 2010-07-01 2010-07-01 true Fraction Measured (Fm) for HAP Compounds in Wastewater Streams 8 Table 8 to Subpart GGG of Part 63 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES...

  12. 40 CFR Table 8 to Subpart Ggg of... - Fraction Measured (Fm) for HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 12 2014-07-01 2014-07-01 false Fraction Measured (Fm) for HAP Compounds in Wastewater Streams 8 Table 8 to Subpart GGG of Part 63 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES...

  13. 40 CFR Table 8 to Subpart Ggg of... - Fraction Measured (Fm) for HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 12 2012-07-01 2011-07-01 true Fraction Measured (Fm) for HAP Compounds in Wastewater Streams 8 Table 8 to Subpart GGG of Part 63 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES...

  14. Laccases to take on the challenge of emerging organic contaminants in wastewater.

    PubMed

    Gasser, Christoph A; Ammann, Erik M; Shahgaldian, Patrick; Corvini, Philippe F-X

    2014-12-01

    The removal of emerging organic contaminants from municipal wastewater poses a major challenge unsatisfactorily addressed by present wastewater treatment processes. Enzyme-catalyzed transformation of emerging organic contaminants (EOC) has been proposed as a possible solution to this major environmental issue more than a decade ago. Especially, laccases gained interest in this context in recent years due to their broad substrate range and since they only need molecular oxygen as a cosubstrate. In order to ensure the stability of the enzymes and allow their retention and reuse, either immobilization or insolubilization of the biocatalysts seems to be the prerequisite for continuous wastewater treatment applications. The present review summarizes the research conducted on EOC transformation with laccases and presents an overview of the possible immobilization techniques. The goal is to assess the state of the art and identify the next necessary steps that have to be undertaken in order to implement laccases as a tertiary wastewater treatment process in sewage treatment plants. PMID:25359481

  15. Treatment of table olive processing wastewaters using novel photomodified ultrafiltration membranes as first step for recovering phenolic compounds.

    PubMed

    Garcia-Ivars, Jorge; Iborra-Clar, Maria-Isabel; Alcaina-Miranda, Maria-Isabel; Mendoza-Roca, José-Antonio; Pastor-Alcańiz, Laura

    2015-06-15

    Table olive processing wastewaters (TOPW) have high salt concentration and total phenolic content (TPC) causing many environmental problems. To reduce them, ultrafiltration (UF) was applied for treating TOPW. However, NaCl, which is the main responsible of salinity in TOPW, and phenols are small molecules that cannot be separated by conventional UF membranes. They have serious problems caused by fouling, which can be overcome using membrane modification techniques. For these reasons, photomodification may be an effective technique to obtain a stream rich in TPC due to the changes in membrane surface properties. UV-modification in the presence of two hydrophilic compounds (polyethylene glycol and aluminium oxide) was performed to achieve membranes with high reductions of organic matter and to keep the TPC as high as possible. Commercial polyethersulfone (PES) membranes of 30 kDa were used. Surface modification was evaluated using FTIR-ATR spectroscopy and membrane performance was studied by calculating the rejection ratios of colour, chemical oxygen demand (COD) and TPC. Results demonstrated that UF is a useful pre-treatment to reduce organic matter from TOPW, obtaining a permeate rich in TPC. PES/Al2O3 membranes displayed superior antifouling properties and rejection values, keeping high the TPC (>95%). Therefore, UF using modified membranes is an appropriate and sustainable technique for treating TOPW. PMID:25744202

  16. Soil amino compound and carbohydrate contents influenced by organic amendments

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Amino compounds (i. e. amino acids and sugars), and carbohydrates are labile organic components and contribute to the improvement of soil fertility and quality. Animal manure and other organic soil amendments are rich in both amino compounds and carbohydrates, hence organic soil amendments might af...

  17. Occurrence of pharmaceuticals and other organic wastewater constituents in selected streams in northern Arkansas, 2004

    USGS Publications Warehouse

    Galloway, Joel M.; Haggard, Brian E.; Meyers, Michael T.; Green, W. Reed

    2005-01-01

    The U.S. Geological Survey, in cooperation with the University of Arkansas and the U.S. Department of Agriculture, Agricultural Research Service, collected data in 2004 to determine the occurrence of pharmaceuticals and other organic wastewater constituents, including many constituents of emerging environmental concern, in selected streams in northern Arkansas. Samples were collected in March and April 2004 from 17 sites located upstream and downstream from wastewater- treatment plant effluent discharges on 7 streams in northwestern Arkansas and at 1 stream site in a relatively undeveloped basin in north-central Arkansas. Additional samples were collected at three of the sites in August 2004. The targeted organic wastewater constituents and sample sites were selected because wastewater-treatment plant effluent discharge provides a potential point source of these constituents and analytical techniques have improved to accurately measure small amounts of these constituents in environmental samples. At least 1 of the 108 pharmaceutical or other organic wastewater constituents was detected at all sites in 2004, except at Spavinaw Creek near Maysville, Arkansas. The number of detections generally was greater at sites downstream from municipal wastewater-treatment plant effluent discharges (mean = 14) compared to sites not influenced by wastewatertreatment plants (mean = 3). Overall, 42 of the 108 constituents targeted in the collected water-quality samples were detected. The most frequently detected constituents included caffeine, phenol, para-cresol, and acetyl hexamethyl tetrahydro naphthalene.

  18. 75 FR 24404 - Approval and Promulgation of Air Quality Implementation Plans; Indiana; Volatile Organic Compound...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-05-05

    ...approved volatile organic compound (VOC) automobile refinishing...requirements, Volatile organic compounds. Dated: March 31, 2010...approved volatile organic compound (VOC) automobile refinishing...Article 8: Volatile Organic Compound Rules, Rule 10:...

  19. 76 FR 18893 - Approval and Promulgation of Air Quality Implementation Plans; Ohio; Volatile Organic Compound...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-04-06

    ...printing volatile organic compound (VOC) rule. These rule...requirements, Volatile organic compounds. Dated: March 10, 2011...printing volatile organic compound (VOC) rule for approval...Control of volatile organic compound emissions from offset...

  20. Method and reaction pathway for selectively oxidizing organic compounds

    DOEpatents

    Camaioni, Donald M. (Richland, WA); Lilga, Michael A. (Richland, WA)

    1998-01-01

    A method of selectively oxidizing an organic compound in a single vessel comprises: a) combining an organic compound, an acid solution in which the organic compound is soluble, a compound containing two oxygen atoms bonded to one another, and a metal ion reducing agent capable of reducing one of such oxygen atoms, and thereby forming a mixture; b) reducing the compound containing the two oxygen atoms by reducing one of such oxygen atoms with the metal ion reducing agent to, 1) oxidize the metal ion reducing agent to a higher valence state, and 2) produce an oxygen containing intermediate capable of oxidizing the organic compound; c) reacting the oxygen containing intermediate with the organic compound to oxidize the organic compound into an oxidized organic intermediate, the oxidized organic intermediate having an oxidized carbon atom; d) reacting the oxidized organic intermediate with the acid counter ion and higher valence state metal ion to bond the acid counter ion to the oxidized carbon atom and thereby produce a quantity of an ester incorporating the organic intermediate and acid counter ion; and e) reacting the oxidized organic intermediate with the higher valence state metal ion and water to produce a quantity of alcohol which is less than the quantity of ester, the acid counter ion incorporated in the ester rendering the carbon atom bonded to the counter ion less reactive with the oxygen containing intermediate in the mixture than is the alcohol with the oxygen containing intermediate.

  1. Oceanic protection of prebiotic organic compounds from UV radiation

    NASA Technical Reports Server (NTRS)

    Cleaves, H. J.; Miller, S. L.; Bada, J. L. (Principal Investigator)

    1998-01-01

    It is frequently stated that UV light would cause massive destruction of prebiotic organic compounds because of the absence of an ozone layer. The elevated UV flux of the early sun compounds this problem. This applies to organic compounds of both terrestrial and extraterrestrial origin. Attempts to deal with this problem generally involve atmospheric absorbers. We show here that prebiotic organic polymers as well as several inorganic compounds are sufficient to protect oceanic organic molecules from UV degradation. This aqueous protection is in addition to any atmospheric UV absorbers and should be a ubiquitous planetary phenomenon serving to increase the size of planetary habitable zones.

  2. Capability of microalgae-based wastewater treatment systems to remove emerging organic contaminants: a pilot-scale study.

    PubMed

    Matamoros, Víctor; Gutiérrez, Raquel; Ferrer, Ivet; García, Joan; Bayona, Josep M

    2015-05-15

    The effect of hydraulic retention time (HRT) and seasonality on the removal efficiency of 26 organic microcontaminants from urban wastewater was studied in two pilot high-rate algal ponds (HRAPs). The targeted compounds included pharmaceuticals and personal care products, fire retardants, surfactants, anticorrosive agents, pesticides and plasticizers, among others. The pilot plant, which was fed at a surface loading rate of 7-29 g of COD m(-2)d(-1), consisted of a homogenisation tank and two parallel lines, each one with a primary settler and an HRAP with a surface area of 1.5 m(2) and a volume of 0.5 m(3). The two HRAPs were operated with different HRTs (4 and 8 d). The removal efficiency ranged from negligible removal to more than 90% depending on the compound. Microcontaminant removal efficiencies were enhanced during the warm season, while the HRT effect on microcontaminant removal was only noticeable in the cold season. Our results suggest that biodegradation and photodegradation are the most important removal pathways, whereas volatilization and sorption were solely achieved for hydrophobic compounds (log Kow>4) with a moderately high Henry's law constant values (11-12 Pa m(-3)mol(-1)) such as musk fragrances. Whereas acetaminophen, ibuprofen and oxybenzone presented ecotoxicological hazard quotients (HQs) higher than 1 in the influent wastewater samples, the HQs for the effluent water samples were always below 1. PMID:25682515

  3. Effect of colloids on the occurrence, distribution and photolysis of emerging organic contaminants in wastewaters.

    PubMed

    Yan, Caixia; Nie, Minghua; Yang, Yi; Zhou, Junliang; Liu, Min; Baalousha, Mohammed; Lead, Jamie R

    2015-12-15

    The effect of colloids on the occurrence, phase distribution and photolysis of twenty-seven emerging organic contaminants (EOCs) was studied in domestic and livestock wastewaters (DW and LW), respectively. Filtered water (<1?m) was separated into permeate (<1kDa) and retentate (1kDa-1?m) by cross flow ultrafiltration. Results indicated that total concentration of EOCs ranged from 1220ngL(-1) in permeate of DW to 5065ngL(-1) in retentate of LW. The average EOC fraction associated with colloids was 13.5% and 14.4% in DW and LW. Most of the EOCs exhibited pseudo-first-order degradation kinetics in all water samples. Control experiments using glass and quartz reactors showed that UV light was more effective on the photolysis of most EOCs. The EOCs photolysis in the three fractions of DW and LW could be accelerated or inhibited compared to ultrapure water with the enhancement factor ranging from -0.94 to 7.33. The impact of colloids on the photolysis of EOCs depended on the compound and the source of water. The photolysis of most EOCs in permeates and filtrates was generally accelerated, while inhibited in the retentates, which could be attributed to the relatively high dissolved organic carbon contents in retentates. PMID:26135483

  4. Bioavailable and biodegradable dissolved organic nitrogen in activated sludge and trickling filter wastewater treatment plants

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A study was carried out to understand the fate of biodegradable dissolved organic nitrogen (BDON) and bioavailable dissolved organic nitrogen (ABDON) along the treatment trains of a wastewater treatment facility (WWTF) equipped with an activated sludge (AS) system and a WWTF equipped with a two-stag...

  5. CHARACTERIZATION OF REUSABLE MUNICIPAL WASTEWATER EFFLUENTS AND CONCENTRATION OF ORGANIC CONSTITUENTS

    EPA Science Inventory

    The main thrust of this project was to collect organic concentrates from operating advanced wastewater treatment (AWT) plants for use in health effects testing. A reverse osmosis process was employed in the first stage concentration; the organics were further concentrated and rec...

  6. GC/MS METHODOLOGY FOR PRIORITY ORGANICS IN MUNICIPAL WASTEWATER TREATMENT

    EPA Science Inventory

    A state-of-the-art review is presented on the current GC/MS methodology for the analysis of priority toxic organics in municipal wastewater treatment. The review summarizes both recent published and unpublished literature on GC/MS methods for analysis of toxic organics in municip...

  7. Wet air oxidation of resorcinol as a model treatment for refractory organics in wastewaters from the wood processing industry.

    PubMed

    Weber, Bernd; Chavez, Alma; Morales-Mejia, Julio; Eichenauer, Sabrina; Stadlbauer, Ernst A; Almanza, Rafael

    2015-09-15

    Wastewater treatment systems are important tools to enhance sustainability in terms of reducing environmental impact and complying with sanitary requirements. This work addresses the wet air oxidation (WAO) process for pre-treatment of phenolic wastewater effluents. The aim was to increase biodegradability prior to a subsequent anaerobic stage. In WAO laboratory experiments using a micro-autoclave, the model compound resorcinol was degraded under different oxygen availability regims within the temperature range 150 °C-270 °C. The activation energy was determined to be 51.5 kJ/mol. Analysis of the products revealed that after 3 h of reaction at 230 °C, 97.5% degradation of resorcinol was achieved. At 250 °C and the same reaction time complete removal of resorcinol was observed. In this case the total organic carbon content was reduced down to 29%, from 118.0 mg/L down to 34.4 mg/L. Under these process conditions, the pollutant was only partially mineralized and the ratio of the biological oxygen demand relative to the chemical oxygen demand, which is 0.07 for resorcinol, was increased to a value exceeding 0.5. The main by-product acetic acid, which is a preferred compound for methanogenic bacteria, was found to account for 33% of the total organic carbon. PMID:26164636

  8. WASTE TREATABILITY TESTS OF SPENT SOLVENT AND OTHER ORGANIC WASTEWATERS

    EPA Science Inventory

    Some commercial and industrial facilities treat RCRA spent solvent wastewaters by steam stripping, carbon adsorption, and/or biological processes. Thirteen facilities were visited by EPA's Office of Research and Development (ORD) from June 1985 to September 1986, to conduct sampl...

  9. FIELD SCREENING FOR HALOGENATED VOLATILE ORGANIC COMPOUNDS

    SciTech Connect

    John F. Schabron; Joseph F. Rovani Jr.; Theresa M. Bomstad

    2002-06-01

    Western Research Institute (WRI) initiated exploratory work towards the development of new field screening methodology and a test kit to measure halogenated volatile organic compounds (VOCs) in the field. Heated diode and corona discharge sensors are commonly used to detect leaks of refrigerants from air conditioners, freezers, and refrigerators. They are both selective to the presence of carbon-halogen bonds. Commercially available heated diode and corona discharge leak detectors were procured and evaluated for halogenated VOC response. The units were modified to provide a digital readout of signal related to VOC concentration. Sensor response was evaluated with carbon tetrachloride and tetrachloroethylene (perchloroethylene, PCE), which represent halogenated VOCs with and without double bonds. The response characteristics were determined for the VOCs directly in headspace in Tedlar bag containers. Quantitation limits in air were estimated. Potential interferences from volatile hydrocarbons, such as toluene and heptane, were evaluated. The effect of humidity was studied also. The performance of the new devices was evaluated in the laboratory by spiking soil samples and monitoring headspace for halogenated VOCs. A draft concept of the steps for a new analytical method was outlined. The results of the first year effort show that both devices show potential utility for future analytical method development work towards the goal of developing a portable test kit for screening halogenated VOCs in the field.

  10. Volatile organic compound remedial action project

    SciTech Connect

    1991-12-01

    This Environmental Assessment (EA) reviews a proposed project that is planned to reduce the levels of volatile organic compound (VOC) contaminants present in the Mound domestic water supply. The potable and industrial process water supply for Mound is presently obtained from a shallow aquifer via on-site production wells. The present levels of VOCs in the water supply drawn from the on-site wells are below the maximum contaminant levels (MCLs) permissible for drinking water under Safe Drinking Water Act (SDWA; 40 CFR 141); however, Mound has determined that remedial measures should be taken to further reduce the VOC levels. The proposed project action is the reduction of the VOC levels in the water supply using packed tower aeration (PTA). This document is intended to satisfy the requirements of the National Environmental Policy Act (NEPA) of 1969 and associated Council on Environmental Quality regulations (40 CFR parts 1500 through 1508) as implemented through U.S. Department of Energy (DOE) Order 5440.1D and supporting DOE NEPA Guidelines (52 FR 47662), as amended (54 FR 12474; 55 FR 37174), and as modified by the Secretary of Energy Notice (SEN) 15-90 and associated guidance. As required, this EA provides sufficient information on the probable environmental impacts of the proposed action and alternatives to support a DOE decision either to prepare an Environmental Impact Statement (EIS) or issue a Finding of No Significant Impact (FONSI).

  11. Volatile Organic Compound Emissions by Agricultural Crops

    NASA Astrophysics Data System (ADS)

    Ormeno, E.; Farres, S.; Gentner, D.; Park, J.; McKay, M.; Karlik, J.; Goldstein, A.

    2008-12-01

    Biogenic Volatile Organic Compounds (BVOCs) participate in ozone and aerosol formation, and comprise a substantial fraction of reactive VOC emission inventories. In the agriculturally intensive Central Valley of California, emissions from crops may substantially influence regional air quality, but emission potentials have not been extensively studied with advanced instrumentation for many important crops. Because crop emissions may vary according to the species, and California emission inventories are constructed via a bottom-up approach, a better knowledge of the emission rate at the species-specific level is critical for reducing uncertainties in emission inventories and evaluating emission model performance. In the present study we identified and quantified the BVOCs released by dominant agricultural crops in California. A screening study to investigate both volatile and semivolatile BVOC fractions (oxygenated VOCs, isoprene, monoterepenes, sesquiterpenes, etc.) was performed for 25 crop species (at least 3 replicates plants each), including branch enclosures of woody species (e.g. peach, mandarin, grape, pistachio) and whole plant enclosures for herbaceous species (e.g. onion, alfalfa, carrot), through a dynamic cuvette system with detection by PTRMS, in-situ GCMS/FID, and collection on carbon-based adsorbents followed by extraction and GCMS analysis. Emission data obtained in this study will allow inclusion of these crops in BVOC emission inventories and air quality simulations.

  12. Relative Stabilities of Organic Compounds Using Benson's Additivity Rules.

    ERIC Educational Resources Information Center

    Vitale, Dale E.

    1986-01-01

    Shows how the structure-energy principle can be presented in organic chemistry (without having to resort to quantum mechanics) by use of Benson's Additive Rules. Examples of the application to several major classes of organic compounds are given.

  13. POTENTIAL EMISSIONS OF HAZARDOUS ORGANIC COMPOUNDS FROM SEWAGE SLUDGE INCINERATION

    EPA Science Inventory

    Laboratory thermal decomposition studies were undertaken to evaluate potential organic emissions from sewage sludge incinerators. Precisely controlled thermal decomposition experiments were conducted on sludge spiked with mixtures of hazardous organic compounds, on the mixtures o...

  14. SORPTION OF ORGANIC ACID COMPOUNDS TO SEDIMENTS: INITIAL MODEL DEVELOPMENT

    EPA Science Inventory

    The adsorption to sediments and soils of selected organic acid compounds was examined as a function of compound and sediment properties. ntrinsic compound properties examined included the dissociation constant (pKa) and hydrophobic character. roperties of the sediment examined in...

  15. DEMONSTRATION BULLETIN: ZENOGEM™ WASTEWATER TREATMENT PROCESS - ZENON ENVIRONMENTAL SYSTEMS

    EPA Science Inventory

    Zenon Environmental Systems (Zenon) has developed the ZenoGem™ process to remove organic compounds from wastewater by integrating biological treatment and membrane-based ultrafiltration. This innovative system combines biological treatment to remove biodegradable organic compou...

  16. Removal of dissolved organic matter in water-hyacinth waste-water treatment lagoons

    SciTech Connect

    Victoria-Rueda, C.H.

    1991-01-01

    Secondary treatment of domestic wastewater in water hyacinth lagoons was evaluated under experimental conditions to assess the role of the roots' bacterial biofilm in the removal of dissolved organic matter (DOM). Research was conducted to (1) quantify removal rates by the biofilm as a function of bulk DOM concentration, (2) formulate an analytical model of DOM removal incorporating biofilm activity, and (3) test the model response to variable organic loads in a pilot-scale plant. Removal of DOM by the biofilm was quantified in continuous-flow water hyacinth tanks at ten concentrations ranging from 45 to 330 g COD m {sup {minus}3} . Total DOM removal in the denitrifying, acetate-based experimental system was measured and partitioned into two fractions associated with the activity of biofilm and suspended bacteria. Calculated DOM removal by the biofilm was adjusted for the release of organic compounds by debris decomposition. Values of DOM removal were used to calculate oxygen transfer rates from the water hyacinth roots. A model of DOM removal in water hyacinth lagoons was formulated. The model, composed of four differential equations, was solved at steady-state conditions and the validity of its simulation results was tested in pilot-scale tanks. Hydraulic detection times ranging from 2 to 28 days were evaluated using biofilm density and concentrations of DOM and particulate organics as monitoring parameters of the model response. The observed decrease of suspended bacterial biomass along the tank was correctly simulated by the model, but predictions of effluent concentrations were not always consistent. Predicted values of biofilm bacterial mass were similar to those measured in the tanks, except when large algal populations were present in the film.

  17. Removal of organics and degradation products from industrial wastewater by a membrane bioreactor integrated with ozone or UV/H?O? treatment.

    PubMed

    Laera, G; Cassano, D; Lopez, A; Pinto, A; Pollice, A; Ricco, G; Mascolo, G

    2012-01-17

    The treatment of a pharmaceutical wastewater resulting from the production of an antibacterial drug (nalidixic acid) was investigated employing a membrane bioreactor (MBR) integrated with either ozonation or UV/H(2)O(2) process. This was achieved by placing chemical oxidation in the recirculation stream of the MBR. A conventional configuration with chemical oxidation as polishing for the MBR effluent was also tested as a reference. The synergistic effect of MBR when integrated with chemical oxidation was assessed by monitoring (i) the main wastewater characteristics, (ii) the concentration of nalidixic acid, (iii) the 48 organics identified in the raw wastewater and (iv) the 55 degradation products identified during wastewater treatment. Results showed that MBR integration with ozonation or UV/H(2)O(2) did not cause relevant drawbacks to both biological and filtration processes, with COD removal rates in the range 85-95%. Nalidixic acid passed undegraded through the MBR and was completely removed in the chemical oxidation step. Although the polishing configuration appeared to give better performances than the integrated system in removing 15 out of 48 secondary organics while similar removals were obtained for 19 other compounds. The benefit of the integrated system was however evident for the removal of the degradation products. Indeed, the integrated system allowed higher removals for 34 out of 55 degradation products while for only 4 compounds the polishing configuration gave better performance. Overall, results showed the effectiveness of the integrated treatment with both ozone and UV/H(2)O(2). PMID:22136062

  18. A Systematic Presentation of Organic Phosphorus and Sulfur Compounds.

    ERIC Educational Resources Information Center

    Hendrickson, James B.

    1985-01-01

    Because the names, interrelations, and oxidation levels of the organic compounds of phosphorus and sulfur tend to confuse students, a simple way to organize these compounds has been developed. The system consists of grouping them by oxidation state and extent of carbon substitution. (JN)

  19. 40 CFR 60.582 - Standard for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 2011-07-01 false Standard for volatile organic compounds. 60.582 Section 60.582 Protection...Coating and Printing § 60.582 Standard for volatile organic compounds. (a) On and after the date on which...

  20. 40 CFR 60.452 - Standard for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 2011-07-01 false Standard for volatile organic compounds. 60.452 Section 60.452 Protection...Large Appliances § 60.452 Standard for volatile organic compounds. On or after the date on which the...

  1. 40 CFR 60.442 - Standard for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 2011-07-01 false Standard for volatile organic compounds. 60.442 Section 60.442 Protection...Coating Operations § 60.442 Standard for volatile organic compounds. (a) On and after the date on which...

  2. 40 CFR 60.492 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 2011-07-01 false Standards for volatile organic compounds. 60.492 Section 60.492 Protection...Coating Industry § 60.492 Standards for volatile organic compounds. On or after the date on which the...

  3. 40 CFR 60.392 - Standards for volatile organic compounds

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 2011-07-01 false Standards for volatile organic compounds 60.392 Section 60.392 Protection of...Coating Operations § 60.392 Standards for volatile organic compounds On and after the date on which the...

  4. TEMPORAL VARIABILITY MEASUREMENT OF SPECIFIC VOLATILE ORGANIC COMPOUNDS

    EPA Science Inventory

    Methodology was developed to determine unambiguously trace levels of volatile organic compounds as they vary in concentration over a variety of time scales. his capability is important because volatile organic compounds (VOCs) are usually measure by time-integrative techniques th...

  5. 40 CFR 60.582 - Standard for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standard for volatile organic compounds. 60.582 Section 60.582 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Flexible Vinyl and Urethane Coating and Printing § 60.582 Standard for volatile organic compounds. (a)...

  6. 40 CFR 60.452 - Standard for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for volatile organic compounds. 60.452 Section 60.452 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Industrial Surface Coating: Large Appliances § 60.452 Standard for volatile organic compounds. On or...

  7. 40 CFR 60.712 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standards for volatile organic compounds. 60.712 Section 60.712 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Magnetic Tape Coating Facilities § 60.712 Standards for volatile organic compounds. Each owner or...

  8. 40 CFR 60.582 - Standard for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for volatile organic compounds. 60.582 Section 60.582 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Flexible Vinyl and Urethane Coating and Printing § 60.582 Standard for volatile organic compounds. (a)...

  9. 40 CFR 60.492 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standards for volatile organic compounds. 60.492 Section 60.492 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Beverage Can Surface Coating Industry § 60.492 Standards for volatile organic compounds. On or after...

  10. 40 CFR 60.462 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standards for volatile organic compounds. 60.462 Section 60.462 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Coil Surface Coating § 60.462 Standards for volatile organic compounds. (a) On and after the date...

  11. 40 CFR 60.742 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standards for volatile organic compounds. 60.742 Section 60.742 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Polymeric Coating of Supporting Substrates Facilities § 60.742 Standards for volatile organic compounds....

  12. 40 CFR 60.722 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standards for volatile organic compounds. 60.722 Section 60.722 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... volatile organic compounds. (a) Each owner or operator of any affected facility which is subject to...

  13. 40 CFR 60.622 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standards for volatile organic compounds. 60.622 Section 60.622 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Petroleum Dry Cleaners § 60.622 Standards for volatile organic compounds. (a) Each affected...

  14. 40 CFR 60.602 - Standard for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standard for volatile organic compounds. 60.602 Section 60.602 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Synthetic Fiber Production Facilities § 60.602 Standard for volatile organic compounds. On and after...

  15. 40 CFR 60.452 - Standard for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standard for volatile organic compounds. 60.452 Section 60.452 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Industrial Surface Coating: Large Appliances § 60.452 Standard for volatile organic compounds. On or...

  16. 40 CFR 60.742 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standards for volatile organic compounds. 60.742 Section 60.742 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Polymeric Coating of Supporting Substrates Facilities § 60.742 Standards for volatile organic compounds....

  17. 40 CFR 60.492 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standards for volatile organic compounds. 60.492 Section 60.492 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Beverage Can Surface Coating Industry § 60.492 Standards for volatile organic compounds. On or after...

  18. 40 CFR 60.462 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standards for volatile organic compounds. 60.462 Section 60.462 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Coil Surface Coating § 60.462 Standards for volatile organic compounds. (a) On and after the date...

  19. 40 CFR 60.722 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standards for volatile organic compounds. 60.722 Section 60.722 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... volatile organic compounds. (a) Each owner or operator of any affected facility which is subject to...

  20. 40 CFR 60.712 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standards for volatile organic compounds. 60.712 Section 60.712 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Magnetic Tape Coating Facilities § 60.712 Standards for volatile organic compounds. Each owner or...

  1. 40 CFR 60.602 - Standard for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for volatile organic compounds. 60.602 Section 60.602 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Synthetic Fiber Production Facilities § 60.602 Standard for volatile organic compounds. On and after...

  2. 40 CFR 60.462 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 2010-07-01 false Standards for volatile organic compounds. 60.462 Section 60.462 Protection of Environment...Surface Coating § 60.462 Standards for volatile organic compounds. (a) On and after the date on which § 60.8...

  3. 40 CFR 60.452 - Standard for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...2010-07-01 2010-07-01 false Standard for volatile organic compounds. 60.452 Section 60.452 Protection of Environment...Large Appliances § 60.452 Standard for volatile organic compounds. On or after the date on which the performance test...

  4. 40 CFR 60.442 - Standard for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...2010-07-01 2010-07-01 false Standard for volatile organic compounds. 60.442 Section 60.442 Protection of Environment...Coating Operations § 60.442 Standard for volatile organic compounds. (a) On and after the date on which the...

  5. 40 CFR 60.622 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 false Standards for volatile organic compounds. 60.622 Section...Cleaners § 60.622 Standards for volatile organic compounds. (a) Each...inspected every 15 days and all vapor or liquid leaks be repaired within the...

  6. REACTIVITY OF NITROGENOUS AND OTHER ORGANIC COMPOUNDS WITH AQUEOUS CHLORINE

    EPA Science Inventory

    A protocol for determining the chlorine demand of organic compounds was developed and tested. Organics were reacted with chlorine at mole ratios of 1:05, 1:1, and 1:3 at pH values of 6, 7, and 8 over a one week period. Compounds tested were drawn mainly from the EPA Register of O...

  7. Comparative toxicity of SRC-I wastewater to aquatic organisms. Final technical report

    SciTech Connect

    Bailey, H.C.

    1984-01-01

    SRI International performed a series of acute and chronic toxicity studies on SRC-I wastewaters using fish, zooplankton, and algae as test organisms. The tests were designed to determine the toxicity of SRC-I wastewaters to quatic organisms and based on differences in toxicity of the various water samples, to evaluate the efficacy of various wastewater treatment methods. Survival data from acute and chronic daphnid studies indicate that phenol recovery markedly reduced wastewater toxicity. In treatment processes that did not include phenol recovery, powdered activated carbon reduced toxicity more effectively than granulated activated carbon. All treated water supported algal growth in excess of that in controls, particularly those waters subjected to phenol recovery. The toxicity of each SRC-I wastewater sample was compared with that of a corresponding synthetic salt solution to determine whether the salt load was the toxic element. The wastewaters typically exhibited higher toxicity than their associated salt solutions. The effect was greatest in the daphnid chronic studies. The aquatic ecotoxicity tests were performed as part of ICRC's post-Base-line environmental R and D program. One objective of the program was to evaluate the impact of phenol recovery on effluent quality. Another objective was to assess the potential impact of wastewater discharge on aquatic organisms. The results of this study have been integrated with results from the rest of the R and D program, and are documented in ICRC's Integration Report for SRC-I Post-Baseline Environmental R and D. 7 references, 10 figures and 22 tables.

  8. Dissolved organic carbon transformations during laboratory-scale groundwater recharge using lagoon-treated wastewater

    SciTech Connect

    Westerhoff, P.; Pinney, M.

    2000-07-01

    Reuse of treated wastewater through groundwater recharge has emerged as an integral part of water and wastewater management in arid regions of the world. Aerated-lagoon wastewater treatment followed by surface infiltration offers a simple low-tech, low-cost treatment option for developing countries. This study investigated the fate of dissolved organic carbon (DOC) through laboratory-scale soil aquifer treatment (SAT) soil columns over a 64-week period. Aerated-lagoon wastewater (average DOE = 17 mg/l) and two soils were collected near the USA/Mexico border near Nogales, AZ. Laboratory-scale SAT columns exhibited three phases of aging where infiltration rates and DOC removals were delineated. DOC removal ranged from 39% to greater than 70% during the study, with DOC levels averaging 3.7 and 5.8 mg/l for the SAT columns packed with different soils. Soil with a higher fraction of organic carbon content had higher effluent DOC levels, presumably due to leaching of soil organic matter. UV absorbance data indicated preferential biodegradation removal of low molecular weight, low aromatic DOC. Overall, SAT reduced the potential towards forming trihalomethanes (THMs) during disinfection, although the reactivity ({mu}g THM/mg DOC) increased. SAT and groundwater recharge would provide a high degree of DOC removal in an integrated low-tech wastewater reuse management strategy, especially for developing countries in arid regions of the world.

  9. Removal of total organic carbon from sewage wastewater using poly(ethylenimine)-functionalized magnetic nanoparticles.

    PubMed

    Lakshmanan, Ramnath; Sanchez-Dominguez, Margarita; Matutes-Aquino, Jose A; Wennmalm, Stefan; Kuttuva Rajarao, Gunaratna

    2014-02-01

    The increased levels of organic carbon in sewage wastewater during recent years impose a great challenge to the existing wastewater treatment process (WWTP). Technological innovations are therefore sought that can reduce the release of organic carbon into lakes and seas. In the present study, magnetic nanoparticles (NPs) were synthesized, functionalized with poly(ethylenimine) (PEI), and characterized using TEM (transmission electron microscopy), X-ray diffraction (XRD), FTIR (Fourier transform infrared spectroscopy), CCS (confocal correlation spectroscopy), SICS (scattering interference correlation spectroscopy), magnetism studies, and thermogravimetric analysis (TGA). The removal of total organic carbon (TOC) and other contaminants using PEI-coated magnetic nanoparticles (PEI-NPs) was tested in wastewater obtained from the Hammarby Sjöstadsverk sewage plant, Sweden. The synthesized NPs were about 12 nm in diameter and showed a homogeneous particle size distribution in dispersion by TEM and CCS analyses, respectively. The magnetization curve reveals superparamagnetic behavior, and the NPs do not reach saturation because of surface anisotropy effects. A 50% reduction in TOC was obtained in 60 min when using 20 mg/L PEI-NPs in 0.5 L of wastewater. Along with TOC, other contaminants such as turbidity (89%), color (86%), total nitrogen (24%), and microbial content (90%) were also removed without significant changes in the mineral ion composition of wastewater. We conclude that the application of PEI-NPs has the potential to reduce the processing time, complexity, sludge production, and use of additional chemicals in the WWTP. PMID:24428551

  10. Hepatotoxicity and nephrotoxicity of organic contaminants in wastewater-irrigated soil.

    PubMed

    Gao, Hongxia; Liu, Yingli; Guan, Weijun; Li, Qingzhao; Liu, Nan; Gao, Zhenjie; Fan, Jianjun

    2015-03-01

    The objective of this study is to investigate the hepatotoxicity and nephrotoxicity of organic contaminants in wastewater-irrigated soil using in vivo and in vitro experiments on mice and rat. Soil samples were collected from a wastewater-irrigated area and groundwater-irrigated area, i.e. clean water-irrigated area as control group. The organic contaminants were extracted using an ultrasonic oscillator. In vivo experiment was performed by contamination of hepatocytes of rat using the organic extract, and comet assay was used to analyse the DNA damage of hepatocytes. For in vitro experiment, mice were first gavaged with extracts, and then the indicators for kidney functions, liver functions and oxidative damage of tissues were investigated. The result shows, for in vitro experiments, compared with clean water-irrigated area groups, the average DNA tailing length for the wastewater-irrigated area group is larger, and for the wastewater-irrigated area groups with extract concentration 0.6 g/ml and 0.9 g/ml, the tailing rate increases significantly (P?wastewater-irrigated area, while both kidney and liver indices decreased for wastewater-irrigated area high-dose group (P?wastewater-irrigated low-dose group and Gamma-glutamyl transpeptidase, creatinine for high-dose group all increased (P?wastewater-irrigated groups and glutathione peroxidase activity for high-dose group, malondialdehyde content all decreased (P?wastewater-irrigated high-dose group decreased (P?wastewater-irrigated soil is able to cause DNA damage of hepatocytes in rats, changes of liver functions in mice and lead to oxidative damage of liver and kidney. PMID:25263415

  11. 75 FR 57390 - Approval and Promulgation of Implementation Plans; Alabama: Volatile Organic Compounds

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-09-21

    ...definition of ``volatile organic compounds'' (VOCs) found...carbon dioxide, carbonic acid, metallic carbides or carbonates...Compounds of carbon (or organic compounds) have different...recordkeeping requirements, Volatile organic compounds. Dated:...

  12. Combined organic matter and nitrogen removal from a chemical industry wastewater in a two-stage MBBR system.

    PubMed

    Cao, S M S; Fontoura, G A T; Dezotti, M; Bassin, J P

    2016-01-01

    Pesticide-producing factories generate highly polluting wastewaters containing toxic and hazardous compounds which should be reduced to acceptable levels before discharge. In this study, a chemical industry wastewater was treated in a pre-denitrification moving-bed biofilm reactor system subjected to an increasing internal mixed liquor recycle ratio from 2 to 4. Although the influent wastewater characteristics substantially varied over time, the removal of chemical oxygen demand (COD) and dissolved organic carbon was quite stable and mostly higher than 90%. The highest fraction of the incoming organic matter was removed anoxically, favouring a low COD/N environment in the subsequent aerobic nitrifying tank and thus ensuring stable ammonium removal (90-95%). However, during pH and salt shock periods, nitrifiers were severely inhibited but gradually restored their full nitrifying capability as non-stressing conditions were reestablished. Besides promoting an increase in the maximum nitrification potential of the aerobic attached biomass from 0.34 to 0.63?mg [Formula: see text], the increase in the internal recycle ratio was accompanied by an increase in nitrogen removal (60-78%) and maximum specific denitrification rate (2.7-3.3?mg [Formula: see text]). Total polysaccharides (PS) and protein (PT) concentrations of attached biomass were observed to be directly influenced by the influent organic loading rate, while the PS/PT ratio mainly ranged from 0.3 to 0.5. Results of Microtox tests showed that no toxicity was found in the effluent of both the anoxic and aerobic reactors, indicating that the biological process was effective in removing residual substances which might adversely affect the receiving waters' ecosystem. PMID:26086717

  13. Removal of volatile organic compounds using amphiphilic cyclodextrin-coated polypropylene

    PubMed Central

    Lumholdt, Ludmilla; Fourmentin, Sophie; Nielsen, Thorbjřrn T

    2014-01-01

    Summary Polypropylene nonwovens were functionalised using a self-assembled, amphiphilic cyclodextrin coating and the potential for water purification by removal of pollutants was studied. As benzene is one of the problematic compounds in the Water Framework Directive, six volatile organic compounds (benzene and five benzene-based substances) were chosen as model compounds. The compounds were tested as a mixture in order to provide a more realistic situation since the wastewater will be a complex mixture containing multiple pollutants. The volatile organic compounds are known to form stable inclusion complexes with cyclodextrins. Six different amphiphilic cyclodextrin derivatives were synthesised in order to elucidate whether or not the uptake abilities of the coating depend on the structure of the derivative. Headspace gas chromatography was used for quantification of the uptake exploiting the volatile nature of benzene and its derivatives. The capacity was shown to increase beyond the expected stoichiometries of guest–host complexes with ratios of up to 16:1. PMID:25550739

  14. FIELD SCREENING FOR HALOGENATED VOLATILE ORGANIC COMPOUNDS

    SciTech Connect

    John F. Schabron; Joseph F. Rovani, Jr.; Theresa M. Bomstad

    2003-07-01

    Western Research Institute (WRI) is continuing work toward the development of new screening methodology and a test kit to measure halogenated volatile organic compounds (VOCs) in the field. Heated diode and corona discharge sensors are commonly used to detect leaks of refrigerants from air conditioners, freezers, and refrigerators. They are both selective to the presence of halogens. In prior work, the devices were tested for response to carbon tetrachloride, heptane, toluene, and water vapors. In the current work, sensor response was evaluated with sixteen halogenated VOCs relative to carbon tetrachloride. The results show that the response of the various chlorinated VOCs is within an order of magnitude of the response to carbon tetrachloride for each of the sensors. Thus, for field screening a single response factor can be used. Both types of leak detectors are being further modified to provide an on-board LCD signal readout, which is related to VOC concentration. The units will be fully portable and will operate with 115-V line or battery power. Signal background, noise level, and response data on the Bacharach heated diode detector and the TIF corona discharge detector show that when the response curves are plotted against the log of concentration, the plot is linear to the upper limit for the particular unit, with some curvature at lower levels. When response is plotted directly against concentration, the response is linear at the low end and is curved at the high end. The dynamic ranges for carbon tetrachloride of the two devices from the lower detection limit (S/N=2) to signal saturation are 4-850 vapor parts per million (vppm) for the corona discharge unit and 0.01-70 vppm for the heated diode unit. Additional circuit modifications are being made to lower the detection limit and increase the dynamic response range of the corona discharge unit. The results indicate that both devices show potential utility for future analytical method development work toward the goal of developing a portable test kit for screening halogenated VOCs in the field.

  15. Pilot-scale study on nitrogen and aromatic compounds removal in printing and dyeing wastewater by reinforced hydrolysis-denitrification coupling process and its microbial community analysis.

    PubMed

    Li, Chao; Ren, Hongqiang; Yin, Erqin; Tang, Siyuan; Li, Yi; Cao, Jiashun

    2015-06-01

    Aiming to efficiently dispose printing and dyeing wastewater with "high organic nitrogen and aromatic compounds, but low carbon source quality", the reinforced anaerobic hydrolysis-denitrification coupling process, based on improved UASB reactors and segregated collection-disposition strategy, was designed and applied at the pilot scale. Results showed that the coupling process displayed efficient removal for these two kinds of pollutants (nitrogen and aromatics), since the concentration of NH3-N (shortened as ? (NH3-N))?compound-degrading potential, which demonstrates that the coupling process owns admirable applicability for this kind of wastewater treatment. PMID:25613804

  16. Attenuation of trace organic compounds (TOrCs) in bioelectrochemical systems.

    PubMed

    Werner, Craig M; Hoppe-Jones, Christiane; Saikaly, Pascal E; Logan, Bruce E; Amy, Gary L

    2015-04-15

    Microbial fuel cells (MFCs) and microbial electrolysis cells (MECs) are two types of microbial bioelectrochemical systems (BESs) that use microorganisms to convert chemical energy in wastewaters into useful energy products such as (bio)electricity (MFC) or hydrogen gas (MEC). These two systems were evaluated for their capacity to attenuate trace organic compounds (TOrCs), commonly found in municipal wastewater, under closed circuit (current generation) and open circuit (no current generation) conditions, using acetate as the carbon source. A biocide was used to evaluate attenuation in terms of biotransformation versus sorption. The difference in attenuation observed before and after addition of the biocide represented biotransformation, while attenuation after addition of a biocide primarily indicated sorption. Attenuation of TOrCs was similar in MFCs and MECs for eight different TOrCs, except for caffeine and trimethoprim where slightly higher attenuation was observed in MECs. Electric current generation did not enhance attenuation of the TOrCs except for caffeine, which showed slightly higher attenuation under closed circuit conditions in both MFCs and MECs. Substantial sorption of the TOrCs occurred to the biofilm-covered electrodes, but no consistent trend could be identified regarding the physico-chemical properties of the TOrCs tested and the extent of sorption. The octanol-water distribution coefficient at pH 7.4 (log DpH 7.4) appeared to be a reasonable predictor for sorption of some of the compounds (carbamazepine, atrazine, tris(2-chloroethyl) phosphate and diphenhydramine) but not for others (N,N-Diethyl-meta-toluamide). Atenolol also showed high levels of sorption despite being the most hydrophilic in the suite of compounds studied (log DpH 7.4 = -1.99). Though BESs do not show any inherent advantages over conventional wastewater treatment, with respect to TOrC removal, overall removals in BESs are similar to that reported for conventional wastewater systems, implying the possibility of using BESs for energy production in wastewater treatment without adversely impacting TOrC attenuations. PMID:25644628

  17. Determination of Wastewater Compounds in Sediment and Soil by Pressurized Solvent Extraction, Solid-Phase Extraction, and Capillary-Column Gas Chromatography/Mass Spectrometry

    USGS Publications Warehouse

    Burkhardt, Mark R.; Zaugg, Steven D.; Smith, Steven G.; ReVello, Rhiannon C.

    2006-01-01

    A method for the determination of 61 compounds in environmental sediment and soil samples is described. The method was developed in response to increasing concern over the effects of endocrine-disrupting chemicals in wastewater and wastewater-impacted sediment on aquatic organisms. This method also may be used to evaluate the effects of combined sanitary and storm-sewer overflow on the water and sediment quality of urban streams. Method development focused on the determination of compounds that were chosen on the basis of their endocrine-disrupting potential or toxicity. These compounds include the alkylphenol ethoxylate nonionic surfactants and their degradates, food additives, fragrances, antioxidants, flame retardants, plasticizers, industrial solvents, disinfectants, fecal sterols, polycyclic aromatic hydrocarbons, and high-use domestic pesticides. Sediment and soil samples are extracted using a pressurized solvent extraction system. The compounds of interest are extracted from interfering matrix components by high-pressure water/isopropyl alcohol extraction. The compounds were isolated using disposable solid-phase extraction (SPE) cartridges containing chemically modified polystyrene-divinylbenzene resin. The cartridges were dried with nitrogen gas, and then sorbed compounds were eluted with methylene chloride (80 percent)-diethyl ether (20 percent) through Florisil/sodium sulfate SPE cartridge, and then determined by capillary-column gas chromatography/mass spectrometry. Recoveries in reagent-sand samples fortified at 4 to 72 micrograms averaged 76 percent ?13 percent relative standard deviation for all method compounds. Initial method reporting levels for single-component compounds ranged from 50 to 500 micrograms per kilogram. The concentrations of 20 out of 61 compounds initially will be reported as estimated with the 'E' remark code for one of three reasons: (1) unacceptably low-biased recovery (less than 60 percent) or highly variable method performance (greater than 25 percent relative standard deviation), (2) reference standards prepared from technical mixtures, or (3) potential blank contamination. Samples were preserved by freezing to -20 degrees Celsius. The U.S. Geological Survey National Water Quality Laboratory has established a 1-year sample-holding time limit (prior to sample extraction) from the date of sample collection (if the sample is kept at -20?C) until a statistically accepted method can be used to determine the effectiveness of the sample-freezing procedure.

  18. TOXIC ORGANIC EMISSIONS FROM SYNFUELS AND RELATED INDUSTRIAL WASTEWATER TREATMENT SYSTEMS

    EPA Science Inventory

    The report gives results of an examination of the potential for toxic organic emissions from synfuels wastewater treatment systems. The synthetic fuels facilities examined were coal gasification, direct and indirect coal liquefaction, shale oil, by-product coke, and associated pe...

  19. EMISSION OF METALS AND ORGANICS FROM MUNICIPAL WASTEWATER SLUDGE INCINERATORS - VOLUME I: SUMMARY REPORT

    EPA Science Inventory

    Emissions of metals and organics from a series of four wastewater sludge incinerators were determined. hree multiple hearth units and one fluidized bed combustor were tested. missions were controlled with a combination of venturi and/or tray impingement scrubbers. ne site incorpo...

  20. SORPTION OF ORGANIC PHOSPHORUS COMPOUNDS IN ATLANTIC COASTAL PLAIN SOILS

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Organic phosphorus (P) can comprise a significant amount of the total P in animal wastes, yet there is little information on the potential for organic P to be transferred from soils to watercourses. We examined the adsorption of organic P compounds to soils typical of the Southeastern U.S., i.e. Bl...

  1. Quantifying commuter exposures to volatile organic compounds

    NASA Astrophysics Data System (ADS)

    Kayne, Ashleigh

    Motor-vehicles can be a predominant source of air pollution in cities. Traffic-related air pollution is often unavoidable for people who live in populous areas. Commuters may have high exposures to traffic-related air pollution as they are close to vehicle tailpipes. Volatile organic compounds (VOCs) are one class of air pollutants of concern because exposure to VOCs carries risk for adverse health effects. Specific VOCs of interest for this work include benzene, toluene, ethylbenzene, and xylenes (BTEX), which are often found in gasoline and combustion products. Although methods exist to measure time-integrated personal exposures to BTEX, there are few practical methods to measure a commuter's time-resolved BTEX exposure which could identify peak exposures that could be concealed with a time-integrated measurement. This study evaluated the ability of a photoionization detector (PID) to measure commuters' exposure to BTEX using Tenax TA samples as a reference and quantified the difference in BTEX exposure between cyclists and drivers with windows open and closed. To determine the suitability of two measurement methods (PID and Tenax TA) for use in this study, the precision, linearity, and limits of detection (LODs) for both the PID and Tenax TA measurement methods were determined in the laboratory with standard BTEX calibration gases. Volunteers commuted from their homes to their work places by cycling or driving while wearing a personal exposure backpack containing a collocated PID and Tenax TA sampler. Volunteers completed a survey and indicated if the windows in their vehicle were open or closed. Comparing pairs of exposure data from the Tenax TA and PID sampling methods determined the suitability of the PID to measure the BTEX exposures of commuters. The difference between BTEX exposures of cyclists and drivers with windows open and closed in Fort Collins was determined. Both the PID and Tenax TA measurement methods were precise and linear when evaluated in the laboratory using standard BTEX gases. The LODs for the Tenax TA sampling tubes (determined with a sample volume of 1,000 standard cubic centimeters which is close to the approximate commuter sample volumes collected) were orders of magnitude lower (0.04 to 0.7 parts per billion (ppb) for individual compounds of BTEX) compared to the PIDs' LODs (9.3 to 15 ppb of a BTEX mixture), which makes the Tenax TA sampling method more suitable to measure BTEX concentrations in the sub-parts per billion (ppb) range. PID and Tenax TA data for commuter exposures were inversely related. The concentrations of VOCs measured by the PID were substantially higher than BTEX concentrations measured by collocated Tenax TA samplers. The inverse trend and the large difference in magnitude between PID responses and Tenax TA BTEX measurements indicates the two methods may have been measuring different air pollutants that are negatively correlated. Drivers in Fort Collins, Colorado with closed windows experienced greater time-weighted average BTEX exposures than cyclists (p: 0.04). Commuter BTEX exposures measured in Fort Collins were lower than commuter exposures measured in prior studies that occurred in larger cities (Boston and Copenhagen). Although route and intake may affect a commuter's BTEX dose, these variables are outside of the scope of this study. Within the limitations of this study (including: small sample size, small representative area of Fort Collins, and respiration rates not taken into account), it appears health risks associated with traffic-induced BTEX exposures may be reduced by commuting via cycling instead of driving with windows closed and living in a less populous area that has less vehicle traffic. Although the PID did not reliably measure low-level commuter BTEX exposures, the Tenax TA sampling method did. The PID measured BTEX concentrations reliably in a controlled environment, at high concentrations (300-800 ppb), and in the absence of other air pollutants. In environments where there could be multiple chemicals present that may produce a PID signal (such a

  2. Enantiomeric and Isotopic Analysis of Organic Compounds in Carbonaceous Meteorites

    NASA Technical Reports Server (NTRS)

    Cooper, George

    2004-01-01

    Carbonaceous meteorites are relatively enriched in soluble organic compounds. The Murchison and Murray meteorites contain numerous compounds of interest in the study of early solar system organic chemistry and organic compounds of potential importance for the origin of life. These include: amino acids, amides, carboxylic acids, and polyols. This talk will focus on the enantiomeric and isotopic analysis of individual meteoritic compounds - primarily polyol acids. The analyses will determine if, in addition to certain amino acids from Murchison, another potentially important class of prebiotic compounds also contains enantiomeric excesses, i.e., excesses that could have contributed to the current homochirality of life. Preliminary enantiomeric and isotopic (C- 13) measurements of Murchison glyceric acid show that it is indeed extraterrestrial. C-13 and D isotope analysis of meteoritic sugar alcohols (glycerol, threitol, ribitol, etc.) has shown that they are also indigenous to the meteorite.

  3. Decomposition of hydrogen peroxide and organic compounds in the presence of iron and iron oxides

    E-print Network

    Kwan, Wai P. (Wai Pang), 1974-

    2003-01-01

    Most advanced oxidation processes use the hydroxyl radical (OH) to treat pollutants found in wastewater and contaminated aquifers because OH reacts with numerous compounds at near diffusion-limited rates. OH can be made ...

  4. Organic compounds in circumstellar and interstellar environments.

    PubMed

    Kwok, Sun

    2015-06-01

    Recent research has discovered that complex organic matter is prevalent throughout the Universe. In the Solar System, it is found in meteorites, comets, interplanetary dust particles, and planetary satellites. Spectroscopic signatures of organics with aromatic/aliphatic structures are also found in stellar ejecta, diffuse interstellar medium, and external galaxies. From space infrared spectroscopic observations, we have found that complex organics can be synthesized in the late stages of stellar evolution. Shortly after the nuclear synthesis of the element carbon, organic gas-phase molecules are formed in the stellar winds, which later condense into solid organic particles. This organic synthesis occurs over very short time scales of about a thousand years. In order to determine the chemical structures of these stellar organics, comparisons are made with particles produced in the laboratory. Using the technique of chemical vapor deposition, artificial organic particles have been created by injecting energy into gas-phase hydrocarbon molecules. These comparisons led us to believe that the stellar organics are best described as amorphous carbonaceous nanoparticles with mixed aromatic and aliphatic components. The chemical structures of the stellar organics show strong similarity to the insoluble organic matter found in meteorites. Isotopic analysis of meteorites and interplanetary dust collected in the upper atmospheres have revealed the presence of pre-solar grains similar to those formed in old stars. This provides a direct link between star dust and the Solar System and raises the possibility that the early Solar System was chemically enriched by stellar ejecta with the potential of influencing the origin of life on Earth. PMID:25720971

  5. Organic Compounds in Circumstellar and Interstellar Environments

    NASA Astrophysics Data System (ADS)

    Kwok, Sun

    2015-06-01

    Recent research has discovered that complex organic matter is prevalent throughout the Universe. In the Solar System, it is found in meteorites, comets, interplanetary dust particles, and planetary satellites. Spectroscopic signatures of organics with aromatic/aliphatic structures are also found in stellar ejecta, diffuse interstellar medium, and external galaxies. From space infrared spectroscopic observations, we have found that complex organics can be synthesized in the late stages of stellar evolution. Shortly after the nuclear synthesis of the element carbon, organic gas-phase molecules are formed in the stellar winds, which later condense into solid organic particles. This organic synthesis occurs over very short time scales of about a thousand years. In order to determine the chemical structures of these stellar organics, comparisons are made with particles produced in the laboratory. Using the technique of chemical vapor deposition, artificial organic particles have been created by injecting energy into gas-phase hydrocarbon molecules. These comparisons led us to believe that the stellar organics are best described as amorphous carbonaceous nanoparticles with mixed aromatic and aliphatic components. The chemical structures of the stellar organics show strong similarity to the insoluble organic matter found in meteorites. Isotopic analysis of meteorites and interplanetary dust collected in the upper atmospheres have revealed the presence of pre-solar grains similar to those formed in old stars. This provides a direct link between star dust and the Solar System and raises the possibility that the early Solar System was chemically enriched by stellar ejecta with the potential of influencing the origin of life on Earth.

  6. Reduction in toxicity of coking wastewater to aquatic organisms by vertical tubular biological reactor.

    PubMed

    Zhou, Siyun; Watanabe, Haruna; Wei, Chang; Wang, Dongzhou; Zhou, Jiti; Tatarazako, Norihisa; Masunaga, Shigeki; Zhang, Ying

    2015-05-01

    We conducted a battery of toxicity tests using photo bacterium, algae, crustacean and fish to evaluate acute toxicity profile of coking wastewater, and to evaluate the performance of a novel wastewater treatment process, vertical tubular biological reactor (VTBR), in the removal of toxicity and certain chemical pollutants. A laboratory scale VTBR system was set up to treat industrial coking wastewater, and investigated both chemicals removal efficiency and acute bio-toxicity to aquatic organisms. The results showed that chemical oxygen demand (COD) and phenol reductions by VTBR were approximately 93% and 100%, respectively. VTBR also reduced the acute toxicity of coking wastewater significantly: Toxicity Unit (TU) decreased from 21.2 to 0.4 for Photobacterium phosphoreum, from 9.5 to 0.6 for Isochrysis galbana, from 31.9 to 1.3 for Daphnia magna, and from 30.0 to nearly 0 for Danio rerio. VTBR is an efficient treatment method for the removal of chemical pollutants and acute bio-toxicity from coking wastewater. PMID:25706086

  7. Phosphatase hydrolysis of organic phosphorus compounds

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Phosphatases are diverse groups of enzymes that deserve special attention because of the significant roles they play in mineralizing organic phosphorus (P) into inorganic available form. For getting more insight on the enzymatically hydrolysis of organic P, in this work, we compared the catalytic pa...

  8. MICROBIAL TRANSFORMATION KINETICS OF ORGANIC COMPOUNDS

    EPA Science Inventory

    One process determining the fate of xenobiotics (organics not natural to a system) in environmental waters is bacterial transformation. Bacteria are one of the most metabolically active groups of organisms in the environment. They can degrade and derive energy from a variety of o...

  9. Evaluating the treatment of a synthetic wastewater containing a pharmaceutical and personal care product chemical cocktail: compound removal efficiency and effects on juvenile rainbow trout.

    PubMed

    Osachoff, Heather L; Mohammadali, Mehrnoush; Skirrow, Rachel C; Hall, Eric R; Brown, Lorraine L Y; van Aggelen, Graham C; Kennedy, Christopher J; Helbing, Caren C

    2014-10-01

    Pharmaceutical and personal care products (PPCPs) can evade degradation in sewage treatment plants (STPs) and can be chronically discharged into the environment, causing concern for aquatic organisms, wildlife, and humans that may be exposed to these bioactive chemicals. The ability of a common STP process, conventional activated sludge (CAS), to remove PPCPs (caffeine, di(2-ethylhexyl)phthalate, estrone, 17?-ethinylestradiol, ibuprofen, naproxen, 4-nonylphenol, tonalide, triclocarban and triclosan) from a synthetic wastewater was evaluated in the present study. The removal of individual PPCPs by the laboratory-scale CAS treatment plant ranged from 40 to 99.6%. While the efficiency of removal for some compounds was high, remaining quantities have the potential to affect aquatic organisms even at low concentrations. Juvenile rainbow trout (Oncorhynchus mykiss) were exposed to influent recreated model wastewater with methanol (IM, solvent control) or with PPCP cocktail (IC), or CAS-treated effluent wastewater with methanol (EM, treated control) or with PPCP cocktail (EC). Alterations in hepatic gene expression (evaluated using a quantitative nuclease protection plex assay) and plasma vitellogenin (VTG) protein concentrations occurred in exposed fish. Although there was partial PPCP removal by CAS treatment, the 20% lower VTG transcript levels and 83% lower plasma VTG protein concentration found in EC-exposed fish compared to IC-exposed fish were not statistically significant. Thus, estrogenic activity found in the influent was retained in the effluent even though typical percent removal levels were achieved raising the issue that greater reduction in contaminant load is required to address hormone active agents. PMID:24963889

  10. GLOBAL INVENTORY OF VOLATILE ORGANIC COMPOUND EMISSIONS FROM ANTHROPOGENIC SOURCES

    EPA Science Inventory

    The paper discusses the development of a global inventory of anthropogenic volatile organic compound (VOC) emissions. t includes VOC estimates for seven classes of VOCs: paraffins, olefins, aromatics (benzene, toluene, xylene), formaldehyde, other aldehydes, other aromatics, and ...

  11. SYNTHESIZING ORGANIC COMPOUNDS USING LIGHT-ACTIVATED TIO2

    EPA Science Inventory

    High-value organic compounds have been synthesized successfully from linear and cyclic hydrocarbons, by photocatalytic oxidation using a semiconductor material, titanium dioxide (TiO2). Various hydrocarbons were partially oxgenated in both liquid and gaseous phase reactors usi...

  12. Synthesis of fluorinated organic compounds using oxygen difluoride

    NASA Technical Reports Server (NTRS)

    Toy, M. S.

    1971-01-01

    Oxygen difluoride synthesis is a much simpler, higher-yield procedure than reactions originally followed to synthesize various fluorinated organic compounds. Extreme care is taken in working with oxygen difluoride as its reactions present severe explosion hazard.

  13. SEPARATION OF VOLATILE ORGANIC COMPOUNDS FROM SURFACTANT SOLUTIONS BY PERVAPORATION

    EPA Science Inventory

    Pervaporation is gradually becoming an accepted and practical method for the recovery of volatile organic compounds (VOCs) from aqueous process and waste streams. As the technolog has matured, new applications for pervaporation have emerged. One such application is the separati...

  14. ESTIMATION OF PHYSIOCHEMICAL PROPERTIES OF ORGANIC COMPOUNDS BY SPARC

    EPA Science Inventory

    The computer program SPARC (SPARC Performs Automated Reasoning in Chemistry) has been under development for several years to estimate physical properties and chemical reactivity parameters of organic compounds strictly from molecular structure. SPARC uses computational algorithms...

  15. ODOR AND IRRITATION EFFECTS OF A VOLATILE ORGANIC COMPOUND MIXTURE

    EPA Science Inventory

    Human exposure to volatile organic compounds elicits a variety ofsymptoms, many of which are thought to be mediated by the olfactoryand trigeminal systems. his report describes evidence indicatingthat perceived odor intensity diminishes during prolonged exposure,whearas irritatin...

  16. 40 CFR 60.712 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... Magnetic Tape Coating Facilities § 60.712 Standards for volatile organic compounds. Each owner or operator... (other than a condenser) on a magnetic tape coating operation shall control emissions from the...

  17. 40 CFR 60.712 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... Magnetic Tape Coating Facilities § 60.712 Standards for volatile organic compounds. Each owner or operator... (other than a condenser) on a magnetic tape coating operation shall control emissions from the...

  18. 40 CFR 60.712 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Magnetic Tape Coating Facilities § 60.712 Standards for volatile organic compounds. Each owner or operator... (other than a condenser) on a magnetic tape coating operation shall control emissions from the...

  19. IMPROVEMENT IN AIR TOXICS METHODS FOR VOLATILE ORGANIC COMPOUNDS

    EPA Science Inventory

    Innovative and customized monitoring methods for air toxic volatile organic compounds (VOCs) are being developed for applications in exposure and trends monitoring. This task addresses the following applications of specific interest:

    o Contributions to EPA Regional Monit...

  20. COMPACT, CONTINUOUS MONITORING FOR VOLATILE ORGANIC COMPOUNDS - PHASE I

    EPA Science Inventory

    Improved methods for onsite measurement of multiple volatile organic compounds are needed for process control, monitoring, and remediation. This Phase I SBIR project sets forth an optical measurement method that meets these needs. The proposed approach provides an instantaneous m...

  1. Speciation of volatile organic compounds from poultry production

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The air consent agreement between EPA and large animal feeding operations (AFO) is designed to determine at what level compounds are being emitted from these facilities. However, the methodology used for quantifying total non-methane hydrocarbons and speciation of volatile organic compounds (VOC) n...

  2. VOLATILE ORGANIC COMPOUNDS MEASURED IN DEARS PASSIVE SAMPLERS

    EPA Science Inventory

    A suite of 27 volatile organic compounds (VOCs) were monitored in personal exposures, indoors and outdoors of participant's residences, and at a central community site during the DEARS summer 2004 monitoring season. The list of VOCs focused on compounds typically associated with ...

  3. CHARACTERIZATION OF VOLATILE ORGANIC COMPOUNDS IN AIRBORNE DUST

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Three methods of extracting volatile organic compounds (VOC's) adsorbed on the airborne dust in a swine finishing building were investigated. Airborne dust was collected in pre-baked glass fiber filters (GFF's) and the compounds were extracted by solvent extraction using dichloromethane, solid phas...

  4. INDOOR AIR QUALITY DATA BASE FOR ORGANIC COMPOUNDS

    EPA Science Inventory

    The report gives results of the compilation of a data base for concentrations of organic compounds measured indoors. ased on a review of the literature from 1979 through 1990, the data base contains information on over 220 compounds ranging in molecular weight from 30 to 446. he ...

  5. DESTRUCTION OF VOLATILE ORGANIC COMPOUNDS VIA CATALYTIC INCINERATION

    EPA Science Inventory

    The paper gives results of an investigation of the effect of catalytic incinerator design and operation the destruction of specific volatile organic compounds (VOCs), both singly and in mixtures. A range of operating and design parameters were tested on a wide variety of compound...

  6. Predicting the emission of volatile organic compounds from silage systems

    Technology Transfer Automated Retrieval System (TEKTRAN)

    As a precursor to smog, emission of volatile organic compounds (VOCs) to the atmosphere is an environmental concern in some regions. The major VOC emission source from farms is silage, with emissions coming from the silo face, mixing wagon, and feed bunk. The major compounds emitted are alcohols wit...

  7. Molecular and Enantiomeric Analysis of Organic Compounds in Carbonaceous Meteorites

    NASA Technical Reports Server (NTRS)

    Cooper, George

    2003-01-01

    Carbonaceous meteorites are relatively enriched in carbon. Much of this carbon is in the form of soluble organic compounds. The Murchison and Murray meteorites are the best-characterized carbonaceous meteorites with respect to organic chemistry. Their content of organic compounds has led to an initial understanding of early solar system organic chemistry as well as what compounds may have played a role in the origin of life (Cronin and Chang, 1993). Reported compounds include: amino acids, amides, carboxylic acids, sulfonic acids, and polyols. This talk will focus on the molecular and enantiomeric analysis of individual meteoritic compounds: polyol acids; and a newly identified class of meteorite compounds, keto acids, i.e., acetoacetic acid, levulinic acid, etc. Keto acids (including pyruvic) are critically important in all contemporary organisms. They are key intermediates in metabolism and processes such as the citric acid cycle. Using gas chromatography-mass spectrometry we identified individual meteoritic keto acids after derivatization to one or more of the following forms: isopropyl ester (ISP), trimethyIsiIy1 (TMS), tert-butyldimethylsilyl (BDMS). Ongoing analyses will determine if, in addition to certain amino acids from Murchison (Cronin and Pizzarello, 1997), other potentially important prebiotic compounds also contain enantiomeric excesses, i.e., excesses that could have contributed to the current homochirality of life.

  8. Shock Modifications of Organic Compounds in Carbonaceous Chondrite Parent Bodies

    NASA Technical Reports Server (NTRS)

    Cooper, George W.

    1998-01-01

    Impacts among asteroidal objects would have altered or destroyed pre-existing organic matter in both targets and projectiles to a greater or lesser degree depending upon impact velocities. To begin filling a knowledge gap on the shock metamorphism of organic compounds, we are studying the effects of shock impacts on selected classes of organic compounds utilizing laboratory shock facilities. Our approach is to subject mixtures of organic compounds, embedded in the matrix of the Murchison meteorite, to simulated hypervelocity impacts by firing them into targets at various pressures. The mixtures are then analyzed to determine the amount of each compound that survives as well as to determine if new compounds are being synthesized. The initial compounds added to the matrix (with the exception of thiosulfate). The sulfonic acids were chosen in part because they are relatively abundant in Murchison, relatively stable, and because they and the phosphonic acids are the first well-characterized homologous series of organic sulfur and phosphorus compounds identified in an extraterrestrial material. Experimental procedures were more fully described in the original proposal. A 20 mm gun, with its barrel extending into a vacuum chamber (10(exp -2) torr), was used to launch the projectile containing the sample at approx. 1.6 km/sec (3,600 mi/hr) into the target material. Maximum pressure of impact depend on target/projectile materials. The target was sufficiently thin to assure minimum pressure decay over the total sample thickness.

  9. Process for reducing organic compounds with calcium, amine, and alcohol

    DOEpatents

    Benkeser, R.A.; Laugal, J.A.; Rappa, A.

    1985-08-06

    Olefins are produced by contacting an organic compound having at least one benzene ring with calcium metal, ethylenediamine, a low molecular weight aliphatic alcohol, and optionally a low molecular weight aliphatic primary amine, and/or an inert, abrasive particulate substance. The reduction is conducted at temperatures ranging from about [minus]10 C to about 30 C or somewhat higher. Substantially all of the organic compounds are converted to corresponding cyclic olefins, primarily diolefins.

  10. Process for reducing organic compounds with calcium, amine, and alcohol

    DOEpatents

    Benkeser, Robert A. (West Lafayette, IN); Laugal, James A. (Lostant, IL); Rappa, Angela (Baltimore, MD)

    1985-01-01

    Olefins are produced by contacting an organic compound having at least one benzene ring with calcium metal, ethylenediamine, a low molecular weight aliphatic alcohol, and optionally a low molecular weight aliphatic primary amine, and/or an inert, abrasive particulate substance. The reduction is conducted at temperatures ranging from about -10.degree. C. to about 30.degree. C. or somewhat higher. Substantially all of the organic compounds are converted to corresponding cyclic olefins, primarily diolefins.

  11. ACCEPTED BY WATER ENVIRONMENT RESEARCH ODOR AND VOC REMOVAL FROM WASTEWATER TREATMENT PLANT

    E-print Network

    ACCEPTED BY WATER ENVIRONMENT RESEARCH _______ ODOR AND VOC REMOVAL FROM WASTEWATER TREATMENT PLANT of biofilters for sequential removal of H2S and VOCs from wastewater treatment plant waste air. The biofilter volatile organic compounds (VOCs) and toxic air pollutants emitted from wastewater and solids handling

  12. A laboratory batch reactor test for assessing nonspeciated volatile organic compound biodegradation in activated sludge.

    PubMed

    Cano, M L; Saterbak, A; van Compernolle, R; Williams, M P; Huot, M E; Rhodes, I A; Allen, C C

    2003-01-01

    The relative rates of biodegradation and stripping and volatilization of nonspeciated volatile organic compounds (VOCs) in wastewater treated with aerobic activated-sludge processes can be quantified using a newly developed procedure. This method was adapted from the original aerated draft tube reactor test that was developed to measure biodegradation rate constants for specific volatile pollutants of interest. The original batch test has been modified to include solid-phase microextraction (SPME) fibers for sampling in the gas phase. The experimental procedure using SPME fibers does not require specific identification and quantitation of individual pollutants and can be used to evaluate wastewater with multiple VOCs. To illustrate use of this procedure, laboratory experiments were conducted using biomass and wastewater or effluent from three activated-sludge treatment systems. Each experiment consisted of two trials: a stripping-only trial without biomass and a stripping plus biodegradation trial using biomass from the activated-sludge unit of interest. Data from the two trials were used to quantify the rates of biodegradation by difference. The activated-sludge systems tested were a laboratory diffused-air reactor treating refinery wastewater, a full-scale surface aerated reactor treating a petrochemical wastewater, and a full-scale diffused-air reactor treating a variety of industrial effluents. The biodegradation rate constant data from each laboratory batch experiment were used in model calculations to quantify the fraction emitted (fe) and the fraction biodegraded (fbio) for each system. The fe values ranged from a maximum of 0.01 to a maximum of 0.32, whereas fbio values ranged from a minimum of 0.40 to a minimum 0.95. Two of these systems had been previously tested using a more complicated experimental approach, and the current results were in good agreement with previous results. These results indicate that biodegradation rate constant data from this laboratory method can be successfully used to predict the fate of VOCs in field-scale treatment units, and thus could potentially be used for demonstration of compliance with wastewater VOC emission regulations. PMID:12934828

  13. Thermodynamics of Organic Compound Alteration in Hydrothermal Systems

    NASA Astrophysics Data System (ADS)

    Shock, E. L.

    2005-12-01

    Organic compounds enter hydrothermal systems through infiltrating surface waters, zones of microbial productivity in the subsurface, extracts of organic matter in surrounding host rocks, and abiotic synthesis. Owing to variations in pH, oxidation state, composition, temperature, and pressure throughout the changing pathways of fluid migration over the duration of the system, organic compounds from all of these sources are introduced to conditions where their relative stabilities and reactivities can be dramatically transformed. If those transformations were predictable, then the extent to which organic alteration reactions have occurred could be used to reveal flowpaths and histories of hydrothermal systems. Speciation and mass transfer calculations permit some insight into the underlying thermodynamic driving forces that result in organic compound alteration. As an example, the speciation of many geochemist's canonical organic matter: CH2O depends strongly on oxidation state, temperature, and total concentration of dissolved organic matter. Calculations show that at oxidation states buffered by iron-bearing mineral assemblages, organic acids dominate the speciation of CH2O throughout hydrothermal systems, with acetic acid (itself equivalent to 2 CH2O by bulk composition) and propanoic acid generally the most abundant compounds. However, at more reduced conditions, which may prevail in organic-rich iron-poor sediments, the drive is to form ketones and especially alcohols at the expense of organic acids. The distribution of organic carbon among the various members of these compound classes is strongly dependent on the total concentration of dissolved organic matter. As an example, at a bulk concentration equivalent to average dissolved organic matter in seawater (45?m), the dominant alcohols at 100°C are small compounds like ethanol and 1-propanol. In contrast, at a higher bulk concentration of 500?m, there is a drive to shift large percentages of dissolved organic carbon into 1-pentanol and 1-hexanol. As the fugacity of H2 increases so does the complexity of the mixture of organic compounds that would result in the lowest energy state. However, the number of dominant compounds in the mixture decreases with increasing temperature for similar extents of reduction referenced to mineral buffered conditions.

  14. Load and distribution of organic matter and nutrients in a separated household wastewater stream.

    PubMed

    Todt, Daniel; Heistad, Arve; Jenssen, Petter D

    2015-01-01

    Wastewater from a source-separated sanitation system connected to 24 residential flats was analysed for the content of organic matter and nutrients and other key parameters for microbiological processes used in the treatment and reuse of wastewater. Black water (BW) was the major contributor to the total load of organic matter and nutrients in the wastewater, accounting for 69% of chemical oxygen demand (COD), 83% of total nitrogen (N) and 87% of phosphorus (P). With a low COD/N ratio and high content of free ammonia, treating BW alone is a challenge in traditional biological nitrogen removal approaches. However, its high nitrogen concentration (1.4-1.7?g L(-1)) open up for nutrient reuse as well as for novel, more energy efficient N-removal technologies. Grey water (GW) contained low amounts of nutrients relative to organic matter, and this may limit biological treatment processes under certain conditions. GW contains a higher proportion of soluble, readily degradable organic substances compared with BW, which facilitates simple, decentralized treatment approaches. The concentration of organic matter and nutrients varied considerably between our study and other studies, which could be related to different toilet flushing volumes and water use habits. The daily load per capita, on the other hand, was found to be in line with most of the reported studies. PMID:25495947

  15. Analysis of volatile organic compounds from illicit cocaine samples

    SciTech Connect

    Robins, W.H.; Wright, B.W.

    1994-07-01

    Detection of illicit cocaine hydrochloride shipments can be improved if there is a greater understanding of the identity and quantity of volatile compounds present. This study provides preliminary data concerning the volatile organic compounds detected in a limited Set of cocaine hydrochloride samples. In all cases, cocaine was one of the major volatile compounds detected. Other tropeines were detected in almost all samples. Low concentrations of compounds that may be residues of processing solvents were observed in some samples. The equilibrium emissivity of. cocaine from cocaine hydrochloride was investigated and a value of 83 parts-per-trillion was determined.

  16. Determination of dissolved organic matter removal efficiency in wastewater treatment works using fluorescence spectroscopy

    NASA Astrophysics Data System (ADS)

    Carstea, Elfrida M.; Bridgeman, John

    2015-04-01

    Fluorescence spectroscopy was used to investigate the removal efficiency of dissolved organic matter (DOM) in several wastewater treatment works, at different processing stages. The correlation between fluorescence values and biochemical oxygen demand (BOD), chemical oxygen demand (COD) and total organic carbon (TOC) has been examined. Fluorescence was measured for unfiltered and filtered (0.45 and 0.20 ?m) samples of crude, settled and secondary treated wastewater (activated sludge), and final effluent. Moreover, the potential of using portable fluorimeters has been explored in a laboratory scale activated sludge process. Good correlations were observed for filtered and unfiltered wastewater samples between protein-like fluorescence intensity (excitation 280 nm, emission 350 nm) and BOD (r = 0.78), COD (r = 0.90) and TOC (r = 0.79). BOD displayed a higher correlation at the 0.20 ?m filtered samples compared to COD and TOC. Slightly better relation was seen between fluorescence and conventional parameters at the portable fluorimeters compared to laboratory-based instruments. The results indicated that fluorescence spectroscopy, in particular protein-like fluorescence, could be used for continuous, real-time assessment of DOM removal efficiency in wastewater treatment works.

  17. Biological nitrogen and organic matter removal from tannery wastewater in pilot plant operations in Ethiopia.

    PubMed

    Leta, S; Assefa, F; Gumaelius, L; Dalhammar, G

    2004-12-01

    The objective of this study was to set-up a pilot plant and to evaluate its effectiveness for biological nitrogen and organic matter removal from tannery wastewater in Ethiopia. A pilot wastewater treatment plant consisting of a predenitrification-nitrification process was constructed and operated for 6 months. This was fed with a raw tannery wastewater obtained from the Modjo Tannery located 70 km south of the capital, Addis Ababa. Up to 98% total nitrogen and chemical oxygen demand, and 95% ammonium nitrogen removal efficiencies were achieved in the system. The average effluent ammonium nitrogen ranged from 8.4 mg l(-1) to 86.0 mg l(-1), whereas the average effluent for nitrate nitrogen ranged from 2.9 mg l(-1) to 4.4 mg l(-1). The average values of denitrification and nitrification rates determined by nitrate and ammonium uptake rates (NUR and AUR) were 8.0 mg NO3-N [g volatile suspended solids (VSS)](-1) h(-1) and 5.4 mg NH4-N (g VSS)(-1) h(-1), respectively, demonstrating that the treatment processes of the pilot plant were effective. Further studies of the effect of chromium III on AUR showed 50% inhibition at a concentration of 85 mg l(-1), indicating that this metal was not causing process inhibition during performance operations. Thus, the predenitrification-nitrification process was found to be efficient for simultaneous removal of nitrogen and organic substrates from tannery wastewaters. PMID:15316686

  18. 75 FR 82363 - Approval and Promulgation of Implementation Plans; Ohio; Volatile Organic Compound Emission...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-30

    ...Implementation Plans; Ohio; Volatile Organic Compound Emission Control Measures for Lithographic...letterpress printing volatile organic compound (VOC) rule for approval into the Ohio...recordkeeping requirements, Volatile organic compounds. Dated: December 17, 2010....

  19. 75 FR 2090 - Approval and Promulgation of Air Quality Implementation Plans; Indiana; Volatile Organic Compound...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-01-14

    ...Implementation Plans; Indiana; Volatile Organic Compound Automobile Refinishing Rules for Indiana...Indiana's approved volatile organic compound (VOC) automobile refinishing rules...recordkeeping requirements, Volatile organic compounds. Dated: December 30, 2009....

  20. Seasonal occurrence, removal efficiencies and preliminary risk assessment of multiple classes of organic UV filters in wastewater treatment plants.

    PubMed

    Tsui, Mirabelle M P; Leung, H W; Lam, Paul K S; Murphy, Margaret B

    2014-04-15

    Organic ultraviolet (UV) filters are applied widely in personal care products (PCPs), but the distribution and risks of these compounds in the marine environment are not well known. In this study, the occurrence and removal efficiencies of 12 organic UV filters in five wastewater treatment plants (WWTPs) equipped with different treatment levels in Hong Kong, South China, were investigated during one year and a preliminary environmental risk assessment was carried out. Using a newly developed simultaneous multiclass quantification liquid chromatography-tandem mass spectrometry (LC-MS/MS) method, butyl methoxydibenzoylmethane (BMDM), 2,4-dihydroxybenzophenone (BP-1), benzophenone-3 (BP-3), benzophenone-4 (BP-4) and 2-ethyl-hexyl-4-trimethoxycinnamate (EHMC) were frequently (?80%) detected in both influent and effluent with mean concentrations ranging from 23 to 1290 ng/L and 18-1018 ng/L, respectively; less than 2% of samples contained levels greater than 1000 ng/L. Higher concentrations of these frequently detected compounds were found during the wet/summer season, except for BP-4, which was the most abundant compound detected in all samples in terms of total mass. The target compounds behaved differently depending on the treatment level in WWTPs; overall, removal efficiencies were greater after secondary treatment when compared to primary treatment with >55% and <20% of compounds showing high removal (defined as >70% removal), respectively. Reverse osmosis was found to effectively eliminate UV filters from effluent (>99% removal). A preliminary risk assessment indicated that BP-3 and EHMC discharged from WWTPs may pose high risk to fishes in the local environment. PMID:24503280

  1. Characterizations of organic compounds in diesel exhaust particulates.

    PubMed

    Lim, Jaehyun; Lim, Cheolsoo; Kim, Sangkyun; Hong, Jihyung

    2015-08-01

    To characterize how the speed and load of a medium-duty diesel engine affected the organic compounds in diesel particle matter (PM) below 1?m, four driving conditions were examined. At all four driving conditions, concentration of identifiable organic compounds in PM ultrafine (34-94nm) and accumulation (94-1000nm) modes ranged from 2.9 to 5.7?g/m(3) and 9.5 to 16.4?g/m(3), respectively. As a function of driving conditions, the non-oxygen-containing organics exhibited a reversed concentration trend to the oxygen-containing organics. The identified organic compounds were classified into eleven classes: alkanes, alkenes, alkynes, aromatic hydrocarbons, carboxylic acids, esters, ketones, alcohols, ethers, nitrogen-containing compounds, and sulfur-containing compounds. At all driving conditions, alkane class consistently showed the highest concentration (8.3 to 18.0?g/m(3)) followed by carboxylic acid, esters, ketones and alcohols. Twelve polycyclic aromatic hydrocarbons (PAHs) were identified with a total concentration ranging from 37.9 to 174.8ng/m(3). In addition, nine nitrogen-containing polycyclic aromatic compounds (NPACs) were identified with a total concentration ranging from 7.0 to 10.3ng/m(3). The most abundant PAH (phenanthrene) and NPACs (7,8-benzoquinoline and 3-nitrophenanthrene) comprise a similar molecular (3 aromatic-ring) structure under the highest engine speed and engine load. PMID:26257360

  2. Bioavailability of Dissolved Organic Nitrogen Originating From Natural Sources and Wastewater Effluent in the Truckee River

    NASA Astrophysics Data System (ADS)

    Bertrando, N.; Qualls, R. G.; Dean, K. L.; Springer, M.; Brisbin, M.

    2008-12-01

    It has been suggested that implementation of the Clean Water Act might be further refined to recognize differences in biological availability of Nitrate-N, Ammonium-N, and Dissolved Organic-N (DON) in the regulation of Total Nitrogen (TN) Total Maximum Daily Loads (TMDL). This study was conducted to assess whether wastewater DON has a different bioavailable fraction than natural DON and how the bioavailable fraction of DON in river water varies seasonally across an urban gradient. Since the variety of constituents in DON have not been thoroughly identified and may vary based on source, 67 day bioassays were performed to measure the fraction of DON that is mineralized or converted to particulate matter. To assess the importance of N additions to the Truckee River, algal nutrient limitation assays were performed across the urban gradient. Seasonal bioassays in 2007 demonstrated that wastewater derived DON consistently had a higher bioavailable fraction (23-51 %) than naturally derived DON (~ 0 %). However during summer 2007 the fraction of bioavailable DON was similar for wastewater and natural sources (40 % and 43 %, respectively). DON derived from urban runoff had the highest degree of variation in bioavailability (3-70 %) as opposed to the more consistent bioavailability of wastewater DON. Downstream from the wastewater infall, the bioavailable fraction of DON varied seasonally (0-42 %). Algal nutrient limitation assays demonstrated significant N+P limitation across the urban gradient during the spring and summer but no limitation was observed for winter. A significant N limitation was seen for sites below the urban gradient during the summer season. It appears that wastewater DON consistently has a bioavailable fraction and a recalcitrant fraction (minimum 48 %) which suggests TMDLs could be altered to regulate the bioavailable fraction of TN. The occurrence of N limitation for in-river algal production during the summer season suggests that appropriate N TMDLs are important for this river system. DON bioavailability varies both seasonally and across the urban gradient.

  3. Secondary organic aerosols formed from oxidation of biogenic volatile organic compounds in the Sierra Nevada Mountains of California

    E-print Network

    Goldstein, Allen

    Secondary organic aerosols formed from oxidation of biogenic volatile organic compounds; published 25 August 2006. [1] Biogenic volatile organic compound (BVOC) emissions, such as isoprene that may condense to form secondary organic aerosols (SOA). This research was designed to assess

  4. Highly stable meteoritic organic compounds as markers of asteroidal delivery

    NASA Astrophysics Data System (ADS)

    Cooper, George; Horz, Friedrich; Spees, Alanna; Chang, Sherwood

    2014-01-01

    Multiple missions to search for water-soluble organic compounds on the surfaces of Solar System bodies are either current or planned and, if such compounds were found, it would be desirable to determine their origin(s). Asteroid or comet material is likely to have been components of all surface environments throughout Solar System history. To simulate the survival of meteoritic compounds both during impacts with planetary surfaces and under subsequent (possibly) harsh ambient conditions, we subjected known meteoritic compounds to comparatively high impact-shock pressures (>30 GPa) and/or to extremely oxidizing/corrosive acid solution. Consistent with past impact experiments, ?-amino acids survived only at trace levels above ?18 GPa. Polyaromatic hydrocarbons (PAHs) survived at levels of 4-8% at a shock pressure of 36 GPa. Lower molecular weight sulfonic and phosphonic acids (S&P) had the highest degree of impact survival of all tested compounds at higher pressures. Oxidation of compounds was done with a 3:1 mixture of HCl:HNO3, a solution that generates additional strong oxidants such as Cl2 and NOCl. Upon oxidation, keto acids and ?-amino acids were the most labile compounds with proline as a significant exception. Some fraction of the other compounds, including non-? amino acids and dicarboxylic acids, were stable during 16-18 hours of oxidation. However, S&P quantitatively survived several months (at least) under the same conditions. Such results begin to build a profile of the more robust meteoritic compounds: those that may have survived, i.e., may be found in, the more hostile Solar System environments. In the search for organic compounds, one current mission, NASA's Mars Science Laboratory (MSL), will use analytical procedures similar to those of this study and those employed previously on Earth to identify many of the compounds described in this work. The current results may thus prove to be directly relevant to potential findings of MSL and other missions designed for extraterrestrial organic analysis.

  5. A national reconnaissance of pharmaceuticals and other organic wastewater contaminants in the United States--I) groundwater.

    PubMed

    Barnes, Kimberlee K; Kolpin, Dana W; Furlong, Edward T; Zaugg, Steven D; Meyer, Michael T; Barber, Larry B

    2008-09-01

    As part of the continuing effort to collect baseline information on the environmental occurrence of pharmaceuticals, and other organic wastewater contaminants (OWCs) in the Nation's water resources, water samples were collected from a network of 47 groundwater sites across 18 states in 2000. All samples collected were analyzed for 65 OWCs representing a wide variety of uses and origins. Site selection focused on areas suspected to be susceptible to contamination from either animal or human wastewaters (i.e. down gradient of a landfill, unsewered residential development, or animal feedlot). Thus, sites sampled were not necessarily used as a source of drinking water but provide a variety of geohydrologic environments with potential sources of OWCs. OWCs were detected in 81% of the sites sampled, with 35 of the 65 OWCs being found at least once. The most frequently detected compounds include N,N-diethyltoluamide (35%, insect repellant), bisphenol A (30%, plasticizer), tri(2-chloroethyl) phosphate (30%, fire retardant), sulfamethoxazole (23%, veterinary and human antibiotic), and 4-octylphenol monoethoxylate (19%, detergent metabolite). Although sampling procedures were intended to ensure that all groundwater samples analyzed were indicative of aquifer conditions it is possible that detections of some OWCs could have resulted from leaching of well-construction materials and/or other site-specific conditions related to well construction and materials. Future research will be needed to identify those factors that are most important in determining the occurrence and concentrations of OWCs in groundwater. PMID:18556047

  6. Leveraging the beneficial compounds of organic and pasture milk

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Much discussion has arisen over the possible benefits of organic food, including milk. Organic milk comes from cows that are on pasture during the growing season, and would be expected to contain some compounds that are not found in animals receiving conventional feed, or at higher concentrations. ...

  7. LOSS OF ORGANIC CHEMICALS IN SOIL: PURE COMPOUND TREATABILITY STUDIES

    EPA Science Inventory

    Comprehensive screening data on the treatability of 32 organic chemicals in soil were developed. Of the evaluated chemicals, 22 were phenolic compounds. Aerobic batch laboratory microcosm experiments were conducted using two soils: an acidic clay soil with <1% organic matter and ...

  8. INTERACTIONS BETWEEN ORGANIC COMPOUNDS AND CYCLODEXTRIN-CLAY SYSTEMS

    EPA Science Inventory

    Computational and experimental techniques are combined in order to better understand interactions involving organic compounds and cyclodextrin (CD)-clay systems. CD-clay systems may have great potential in the containment of organic contaminants in the environment. This study w...

  9. Students' Understanding of Molecular Structure and Properties of Organic Compounds.

    ERIC Educational Resources Information Center

    Schmidt, Hans-Jurgen

    The purpose of this study was to investigate senior high school students' difficulties predicting the existence of hydrogen bridge bonds between organic molecules, investigate students' difficulties predicting the relative boiling points of simple organic compounds, and develop test questions that enable teachers to quickly get information about…

  10. 40 CFR 60.392 - Standards for volatile organic compounds

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standards for volatile organic compounds 60.392 Section 60.392 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Automobile and Light Duty Truck Surface Coating Operations § 60.392 Standards for volatile organic...

  11. 40 CFR 60.392 - Standards for volatile organic compounds

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standards for volatile organic compounds 60.392 Section 60.392 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Automobile and Light Duty Truck Surface Coating Operations § 60.392 Standards for volatile organic...

  12. 40 CFR 60.432 - Standard for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for volatile organic compounds. 60.432 Section 60.432 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Graphic Arts Industry: Publication Rotogravure Printing § 60.432 Standard for volatile organic...

  13. 40 CFR 60.432 - Standard for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standard for volatile organic compounds. 60.432 Section 60.432 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Graphic Arts Industry: Publication Rotogravure Printing § 60.432 Standard for volatile organic...

  14. IDENTIFICATION OF ORGANIC COMPOUNDS IN INDUSTRIAL EFFLUENT DISCHARGES

    EPA Science Inventory

    Samples of 63 effluent and 22 intake waters were collected from a wide range of chemical manufacturers in areas across the United States. The samples were analyzed for organic compounds in an effort to identify previously unknown and potentially hazardous organic pollutants. Each...

  15. NONVOLATILE ORGANICS IN DISINFECTED WASTEWATER EFFLUENTS: CHEMICAL CHARACTERIZATION AND MUTAGENICITY

    EPA Science Inventory

    Principal objectives of this research program were to examine the effects of disinfection by chlorine, ozone, and ultraviolet light irradiation on nonvolatile organic constituents in secondary effluents relative to chemical effects and formation of mutagenic substances. In a comp...

  16. Assessment of wastewater treatment plant effluent effects on fish reproduction

    EPA Science Inventory

    Wastewater treatment plant (WWTP) effluents are known contributors of chemical mixtures into the environment. Of particular concern are endocrine-disrupting compounds that can affect hypothalamic-pituitary-gonadal axis function in exposed organisms. The present study examined t...

  17. Photocatalytic fluoroalkylation reactions of organic compounds.

    PubMed

    Barata-Vallejo, Sebastián; Bonesi, Sergio M; Postigo, Al

    2015-12-14

    Photocatalytic methods for fluoroalkyl-radical generation provide more convenient alternatives to the classical perfluoroalkyl-radical (Rf) production through chemical initiators, such as azo or peroxide compounds or the employment of transition metals through a thermal electron transfer (ET) initiation process. The mild photocatalytic reaction conditions tolerate a variety of functional groups and, thus, are handy to the late-stage modification of bioactive molecules. Transition metal-photocatalytic reactions for Rf radical generation profit from the redox properties of coordinatively saturated Ru or Ir organocomplexes to act as both electron donor and reductive species, thus allowing for the utilization of electron accepting and donating fluoroalkylating agents for Rf radical production. On the other hand, laboratory-available and inexpensive photoorgano catalysts (POC), in the absence of transition metals, can also act as electron exchange species upon excitation, resulting in ET reactions that produce Rf radicals. In this work, a critical account of transition metal and transition metal-free Rf radical production will be described with photoorgano catalysts, studying classical examples and the most recent investigations in the field. PMID:26464314

  18. Oxidation of Organic Compounds in the Soil. 

    E-print Network

    Fraps, G. S. (George Stronach)

    1915-01-01

    it. The funnel of the filtering flask was remored and a tightly fitting one-hole r11hl)er stopper was parafined into the opening in the cover. One end of a glass tulle, bent at a right angle, was run through the hole in the stopper down to n... hun- ched grams of qoil (No. 1290) were mixed with 2.5 grams organic ma- terial an? 50 c.c. water. Right jars of each mixture were prepared. In each jar a test tube with a hole in the bottom was inserted to the depth of an inch. One jar of each...

  19. Improving rubber concrete by waste organic sulfur compounds.

    PubMed

    Chou, Liang-Hisng; Lin, Chun-Nan; Lu, Chun-Ku; Lee, Cheng-Haw; Lee, Maw-Tien

    2010-01-01

    In this study, the use of crumb tyres as additives to concrete was investigated. For some time, researchers have been studying the physical properties of concrete to determine why the inclusion of rubber particles causes the concrete to degrade. Several methods have been developed to improve the bonding between rubber particles and cement hydration products (C-S-H) with the hope of creating a product with an improvement in mechanical strength. In this study, the crumb tyres were treated with waste organic sulfur compounds from a petroleum refining factory in order to modify their surface properties. Organic sulfur compounds with amphiphilic properties can enhance the hydrophilic properties of the rubber and increase the intermolecular interaction forces between rubber and C-S-H. In the present study, a colloid probe of C-S-H was prepared to measure these intermolecular interaction forces by utilizing an atomic force microscope. Experimental results showed that rubber particles treated with waste organic sulfur compounds became more hydrophilic. In addition, the intermolecular interaction forces increased with the adsorption of waste organic sulfur compounds on the surface of the rubber particles. The compressive, tensile and flexural strengths of concrete samples that included rubber particles treated with organic sulfur compound also increased significantly. PMID:19710121

  20. Organic micropollutants in rivers downstream of the megacity Beijing: sources and mass fluxes in a large-scale wastewater irrigation system.

    PubMed

    Heeb, Florian; Singer, Heinz; Pernet-Coudrier, Benoît; Qi, Weixiao; Liu, Huijuan; Longrée, Philipp; Müller, Beat; Berg, Michael

    2012-08-21

    The Haihe River System (HRS) drains the Chinese megacities Beijing and Tianjin, forming a large-scale irrigation system severely impacted by wastewater-borne pollution. The origin, temporal magnitudes, and annual mass fluxes of a wide range of pharmaceuticals, household chemicals, and pesticides were investigated in the HRS, which drains 70% of the wastewater discharged by 20 million people living in Beijing. Based on Chinese consumption statistics and our initial screening for 268 micropollutants using high-resolution mass spectrometry, 62 compounds were examined in space and time (2009-2010). The median concentrations ranged from 3 ng/L for metolachlor to 1100 ng/L for benzotriazole and sucralose. Concentrations of carbendazim, clarithromycin, diclofenac, and diuron exceed levels of ecotoxicological concern. Mass-flux analyses revealed that pharmaceuticals (5930 kg/year) and most household chemicals (5660 kg/year) originated from urban wastewaters, while the corrosion inhibitor benzotriazole entered the rivers through other pathways. Total pesticide residues amounted to 1550 kg/year. Per capita loads of pharmaceuticals in wastewater were lower than those in Europe, but are expected to increase in the near future. As 95% of the river water is diverted to irrigate agricultural soil, the loads of polar organic micropollutants transported with the water might pose a serious threat to food safety and groundwater quality. PMID:22845779

  1. Is there a risk for the aquatic environment due to the existence of emerging organic contaminants in treated domestic wastewater? Greece as a case-study.

    PubMed

    Thomaidi, Vasiliki S; Stasinakis, Athanasios S; Borova, Viola L; Thomaidis, Nikolaos S

    2015-02-11

    The ecological threat associated with emerging pollutants detected in wastewater was estimated in country level. Treated wastewater was analyzed for pharmaceuticals and illicit drugs; whereas the concentrations of all emerging contaminants determined in Greek Sewage Treatment Plants were recorded through literature review. Toxicity data was collected after literature review or using ECOSAR and risk quotients (RQs) were calculated for treated wastewater and 25 Greek rivers, for 3 different aquatic organisms (fish, daphnia magna, algae). According to the results, monitoring data was available for 207 micropollutants belonging to 8 different classes. RQ>1 was calculated for 30 compounds in secondary treated wastewater. Triclosan presented RQ>1 (in algae) for all studied rivers; decamethylcyclopentasilane (in daphnia magna), caffeine (in algae) and nonylphenol (in fish) presented RQ>1 in rivers with dilution factors (DF) equal or lower to 1910, 913 and 824, respectively. The class of emerging contaminants that present the greatest threat due to single or mixture toxicity was endocrine disrupters. The mixture of microcontaminants seems to pose significant ecological risk, even in rivers with DF equal to 2388. Future national monitoring programs should include specific microcontaminants that seem to possess environment risk to surface water. PMID:25464317

  2. Oxidation of atmospheric organic carbon : interconnecting volatile organic compounds, intermediate-volatility organic compounds, and organic aerosol

    E-print Network

    Hunter, James Freeman

    2015-01-01

    .Organic molecules have many important roles in the atmosphere, acting as climate and biogeochemical forcers, and in some cases as toxic pollutants. The lifecycle of atmospheric organic carbon is extremely complex, with ...

  3. Solar photo-Fenton using peroxymonosulfate for organic micropollutants removal from domestic wastewater: comparison with heterogeneous TiO? photocatalysis.

    PubMed

    Ahmed, Moussa Mahdi; Brienza, Monica; Goetz, Vincent; Chiron, Serge

    2014-12-01

    This work aims at decontaminating biologically treated domestic wastewater effluents from organic micropollutants by sulfate radical based (SO4(-)) homogeneous photo-Fenton involving peroxymonosulfate as an oxidant, ferrous iron (Fe(II)) as a catalyst and simulated solar irradiation as a light source. This oxidative system was evaluated by using several probe compounds belonging to pesticides (bifenthrin, mesotrione and clothianidin) and pharmaceuticals (diclofenac, sulfamethoxazole and carbamazepine) classes and its kinetic efficiency was compared to that to the well known UV-Vis/TiO2 heterogeneous photocatalysis. Except for carbamazepine, apparent kinetic rate constants were always 10 times higher in PMS/Fe(II)/UV-Vis than in TiO2/UV-Vis system and more than 70% of total organic carbon abatement was reached in less than one hour treatment. Hydroxyl radical (OH) and SO4(-) reactivity was investigated using mesotrione as a probe compound through by-products identification by liquid chromatography-high resolution-mass spectrometry and transformation pathways elucidation. In addition to two OH based transformation pathways, a specific SO4(-) transformation pathway which first involved degradation through one electron transfer oxidation processes followed by decarboxylation were probably responsible for mesotrione degradation kinetic improvement upon UV-Vis/PMS/Fe(II) system in comparison to UVVis/TiO2 system. PMID:25108605

  4. Reconnaissance of selected organic contaminants in effluent and ground water at fifteen municipal wastewater treatment plants in Florida, 1983- 84

    USGS Publications Warehouse

    Pruitt, J.B.; Troutman, D.E.; Irwin, G.A.

    1985-01-01

    Results of a 1983-84 reconnaissance of 15 municipal wastewater treatment plants in Florida indicated that effluent from most of the plants contains trace concentrations of volatile organic compounds. Chloroform was detected in the effluent at 11 of the 15 plants and its common occurrence was likely the result of chlorination. The maximum concentration of chloroform detected in the effluent sampled was 120 micrograms/L. Detectable concentrations of selected organophosphorus insecticides were also common. For example, diazinon was detected in the effluent at 12 of the 15 plants with a maximum concentration of 1.5 micrograms/L. Organochlorine insecticides, primarily lindane, were detected in the effluent at 8 of the 15 plants with a maximum concentration of 1.0 micrograms/L. Volatile compounds, primarily chloroform, were detected in water from monitor wells at four plants and organophosphorus insecticides, primarily diazinon, were present in the groundwater at three treatment plants. Organochlorine insecticides were not detected in any samples from monitor wells. Based on the limited data available, this cursory reconaissance suggests that the organic contaminants commonly occurring in the effluent of many of the treatment plants are not transported into the local groundwater. (Author 's abstract)

  5. Rejection of Trace Organic Compounds by Forward Osmosis Membranes: A Literature Review

    E-print Network

    Treatment Limitations. The prevalence of TOrCs in wastewater effluent and drinking water sources has gainedCs such as organohalogens, organic pesticides, and surfactants. Common examples in water and wastewater treatment include pharmaceuticals, personal care products, disinfection byproducts, and industrial chemicals is of increasing

  6. New Aspects of Zirconium Containing Organic Compounds

    NASA Astrophysics Data System (ADS)

    Marek, Ilan

    Metal carbene complexes have made their way from organometallic curiosities to valuable reagents and catalysts. They offer novel synthetic opportunities in carbon-carbon bond formation based on either carbene-centered reactions or on metal-templated processes which makes them indispensable in modern synthetic methodology. The most prominent metal carbenes are now either commercially available or easy to synthesize and handle with modern laboratory techniques. This volume organized in eight chapters written by the leading scientists in the field illustrates the theoretical background, non-classical nucleophilic and cycloaddition patterns, chromium-templated benzannulation and photo-induced reactions, rhodium-catalyzed carbene transfer as well as the principles and applications of olefin metathesis which has coined the progress in synthetic methodology over the past decade.

  7. GROUNDWATER TRANSPORT OF HYDROPHOBIC ORGANIC COMPOUNDS IN THE PRESENCE OF DISSOLVED ORGANIC MATTER

    EPA Science Inventory

    The effects of dissolved organic matter (DOM) on the transport of hydrophobic organic compounds in soil columns were investigated. Three compounds (naphthalene, phenanthrene and DDT) that spanned three orders of magnitude in water solubility were used. Instead of humic matter, mo...

  8. GROUND WATER TRANSPORT OF HYDROPHOBIC ORGANIC COMPOUNDS IN THE PRESENCE OF DISSOLVED ORGANIC MATTER

    EPA Science Inventory

    The effects of dissolved organic matter (DOM) on the transport of hydrophobic organic compounds in soil columns were investigated. hree compounds (naphthalene, phenathrene, and DDT) that spanned three orders of magnitude in water solubility were used. nstead of humic matter, mole...

  9. Scaffold of Asymmetric Organic Compounds - Magnetite Plaquettes

    NASA Technical Reports Server (NTRS)

    Chan, Q. H. S.; Zolensky, M. E.; Martinez, J.

    2015-01-01

    Life on Earth shows preference towards the set of organics with particular spatial configurations, this 'selectivity' is a crucial criterion for life. With only rare exceptions, life prefers the left- (L-) form over the right- (D-) form of amino acids, resulting in an L-enantiomeric excess (L-ee). Recent studies have shown Lee for alpha-methyl amino acids in some chondrites. Since these amino acids have limited terrestrial occurrence, the origin of their stereoselectivity is nonbiological, and it seems appropriate to conclude that chiral asymmetry, the molecular characteristic that is common to all terrestrial life form, has an abiotic origin. A possible abiotic mechanism that can produce chiral asymmetry in meteoritic amino acids is their formation with the presence of asymmetric catalysts, as mineral crystallization can produce spatially asymmetric structures. Magnetite is shown to be an effective catalyst for the formation of amino acids that are commonly found in chondrites. Magnetite 'plaquettes' (or 'platelets'), first described by Jedwab, show an interesting morphology of barrel-shaped stacks of magnetite disks with an apparent dislocation-induced spiral growth that seem to be connected at the center. A recent study by Singh et al. has shown that magnetites can self-assemble into helical superstructures. Such molecular asymmetry could be inherited by adsorbed organic molecules. In order to understand the distribution of 'spiral' magnetites in different meteorite classes, as well as to investigate their apparent spiral configurations and possible correlation to molecular asymmetry, we observed polished sections of carbonaceous chondrites (CC) using scanning electron microscope (SEM) imaging. The sections were also studied by electron backscattered diffraction (EBSD) in order to reconstruct the crystal orientation along the stack of magnetite disks.

  10. Dosimeter for monitoring vapors and aerosols of organic compounds

    DOEpatents

    Vo-Dinh, Tuan (625 Gulfwood Rd., Knoxville, TN 37923)

    1987-01-01

    A dosimeter is provided for collecting and detecting vapors and aerosols of organic compounds. The dosimeter comprises a lightweight, passive device that can be conveniently worn by a person as a badge or placed at a stationary location. The dosimeter includes a sample collector comprising a porous web treated with a chemical for inducing molecular displacement and enhancing phosphorescence. Compounds are collected onto the web by molecular diffusion. The web also serves as the sample medium for detecting the compounds by a room temperature phosphorescence technique.

  11. Dosimeter for monitoring vapors and aerosols of organic compounds

    DOEpatents

    Vo-Dinh, T.

    1987-07-14

    A dosimeter is provided for collecting and detecting vapors and aerosols of organic compounds. The dosimeter comprises a lightweight, passive device that can be conveniently worn by a person as a badge or placed at a stationary location. The dosimeter includes a sample collector comprising a porous web treated with a chemical for inducing molecular displacement and enhancing phosphorescence. Compounds are collected onto the web by molecular diffusion. The web also serves as the sample medium for detecting the compounds by a room temperature phosphorescence technique. 7 figs.

  12. A national reconnaissance for pharmaceuticals and other organic wastewater contaminants in the United States - II) Untreated drinking water sources

    USGS Publications Warehouse

    Focazio, M.J.; Kolpin, D.W.; Barnes, K.K.; Furlong, E.T.; Meyer, M.T.; Zaugg, S.D.; Barber, L.B.; Thurman, M.E.

    2008-01-01

    Numerous studies have shown that a variety of manufactured and natural organic compounds such as pharmaceuticals, steroids, surfactants, flame retardants, fragrances, plasticizers and other chemicals often associated with wastewaters have been detected in the vicinity of municipal wastewater discharges and livestock agricultural facilities. To provide new data and insights about the environmental presence of some of these chemicals in untreated sources of drinking water in the United States targeted sites were sampled and analyzed for 100 analytes with sub-parts per billion detection capabilities. The sites included 25 ground- and 49 surface-water sources of drinking water serving populations ranging from one family to over 8??million people. Sixty-three of the 100 targeted chemicals were detected in at least one water sample. Interestingly, in spite of the low detection levels 60% of the 36 pharmaceuticals (including prescription drugs and antibiotics) analyzed were not detected in any water sample. The five most frequently detected chemicals targeted in surface water were: cholesterol (59%, natural sterol), metolachlor (53%, herbicide), cotinine (51%, nicotine metabolite), ??-sitosterol (37%, natural plant sterol), and 1,7-dimethylxanthine (27%, caffeine metabolite); and in ground water: tetrachloroethylene (24%, solvent), carbamazepine (20%, pharmaceutical), bisphenol-A (20%, plasticizer), 1,7-dimethylxanthine (16%, caffeine metabolite), and tri (2-chloroethyl) phosphate (12%, fire retardant). A median of 4 compounds were detected per site indicating that the targeted chemicals generally occur in mixtures (commonly near detection levels) in the environment and likely originate from a variety of animal and human uses and waste sources. These data will help prioritize and determine the need, if any, for future occurrence, fate and transport, and health-effects research for subsets of these chemicals and their degradates most likely to be found in water resources used for drinking water in the United States.

  13. TREATMENT OF ORGANIC CHEMICAL MANUFACTURING WASTEWATER FOR REUSE

    EPA Science Inventory

    This research demonstrated the quality of water produced by each step of a state-of-the-art, commercially available process sequence and determined the feasibility and economics of renovating organic chemical watewater for reuse as boiler feedwater or cycle cooling water. The 5-g...

  14. Microbial Removal of the Pharmaceutical Compounds Ibuprofen and Diclofenac from Wastewater

    PubMed Central

    Inderfurth, Nadia; Schraa, Gosse; Kujawa-Roeleveld, Katarzyna; Rijnaarts, Huub

    2013-01-01

    Studies on the occurrence of pharmaceuticals show that the widely used pharmaceuticals ibuprofen and diclofenac are present in relevant concentrations in the environment. A pilot plant treating hospital wastewater with relevant concentrations of these pharmaceuticals was evaluated for its performance to reduce the concentration of the pharmaceuticals. Ibuprofen was completely removed, whereas diclofenac yielded a residual concentration, showing the necessity of posttreatment to remove diclofenac, for example, activated carbon. Successively, detailed laboratory experiments with activated sludge from the same wastewater treatment plant showed bioremediation potential in the treatment plant. The biological degradation pathway was studied and showed a mineralisation of ibuprofen and degradation of diclofenac. The present microbes were further studied in laboratory experiments, and DGGE analyses showed the enrichment and isolation of highly purified cultures that degraded either ibuprofen or diclofenac. This research illuminates the importance of the involved bacteria for the effectiveness of the removal of pharmaceuticals in a wastewater treatment plant. A complete removal of pharmaceuticals from wastewater will stimulate water reuse, addressing the worldwide increasing demand for clean and safe fresh water. PMID:24350260

  15. Simplified Production of Organic Compounds Containing High Enantiomer Excesses

    NASA Technical Reports Server (NTRS)

    Cooper, George W. (Inventor)

    2015-01-01

    The present invention is directed to a method for making an enantiomeric organic compound having a high amount of enantiomer excesses including the steps of a) providing an aqueous solution including an initial reactant and a catalyst; and b) subjecting said aqueous solution simultaneously to a magnetic field and photolysis radiation such that said photolysis radiation produces light rays that run substantially parallel or anti-parallel to the magnetic field passing through said aqueous solution, wherein said catalyst reacts with said initial reactant to form the enantiomeric organic compound having a high amount of enantiomer excesses.

  16. Treatment of hydroponic wastewater by denitrification filters using plant prunings as the organic carbon source.

    PubMed

    Park, J B K; Craggs, R J; Sukias, J P S

    2008-05-01

    This study investigated the feasibility of using pre-treated plant liquors as organic carbon sources for the treatment of hydroponic wastewater containing high nitrate-N (>300 mg N/L). The waste plant material was pre-treated to extract organic carbon-rich liquors. When this plant liquor was used as an organic carbon source in denitrification filters at the organic carbon:nitrogen dose rate of 3C:N, nitrate removal efficiencies were >95% and final effluent nitrate concentrations were consistently <20mg N/L. However, at this dose rate, relatively high concentrations (>140 mg/L) of organic carbon (fBOD5) remained in the final effluents. Therefore, a 'compromise' organic carbon:nitrogen dose rate (2C:N) was trialled, at which nitrate removal efficiencies were maintained at >85%, final effluent nitrate concentrations were consistently below 45 mg N/L, and effluent fBOD5 concentrations were <25mg/L. This study has demonstrated that waste plant material is a suitable carbon source for the removal of nitrate from hydroponic wastewater in a denitrification filter. PMID:17714940

  17. Microalgae and wastewater treatment

    PubMed Central

    Abdel-Raouf, N.; Al-Homaidan, A.A.; Ibraheem, I.B.M.

    2012-01-01

    Organic and inorganic substances which were released into the environment as a result of domestic, agricultural and industrial water activities lead to organic and inorganic pollution. The normal primary and secondary treatment processes of these wastewaters have been introduced in a growing number of places, in order to eliminate the easily settled materials and to oxidize the organic material present in wastewater. The final result is a clear, apparently clean effluent which is discharged into natural water bodies. This secondary effluent is, however, loaded with inorganic nitrogen and phosphorus and causes eutrophication and more long-term problems because of refractory organics and heavy metals that are discharged. Microalgae culture offers an interesting step for wastewater treatments, because they provide a tertiary biotreatment coupled with the production of potentially valuable biomass, which can be used for several purposes. Microalgae cultures offer an elegant solution to tertiary and quandary treatments due to the ability of microalgae to use inorganic nitrogen and phosphorus for their growth. And also, for their capacity to remove heavy metals, as well as some toxic organic compounds, therefore, it does not lead to secondary pollution. In the current review we will highlight on the role of micro-algae in the treatment of wastewater. PMID:24936135

  18. Methods of Analysis by the U.S. Geological Survey National Water Quality Laboratory - Determination of Wastewater Compounds by Polystyrene-Divinylbenzene Solid-Phase Extraction and Capillary-Column Gas Chromatography/Mass Spectrometry

    USGS Publications Warehouse

    Zaugg, Steven D.; Smith, Steven G.; Schroeder, Michael P.; Barber, Larry B.; Burkhardt, Mark R.

    2002-01-01

    A method for the determination of 67 compounds typically found in domestic and industrial wastewater is described. The method was developed in response to increasing concern over the impact of endocrine-disrupting chemicals in wastewater on aquatic organisms. This method also may be useful for evaluating the impact of combined sanitary and storm-sewer overflow on the water quality of urban streams. The method focuses on the determination of compounds that are an indicator of wastewater or that have been chosen on the basis of their endocrine-disrupting potential or toxicity. These compounds include the alkylphenol ethoxylate nonionic surfactants and their degradates, food additives, fragrances, antioxidants, flame retardants, plasticizers, industrial solvents, disinfectants, fecal sterols, polycyclicaromatic hydrocarbons, and high-use domestic pesticides. Water samples are filtered to remove suspended particulate matter and then are extracted by vacuum through disposable solid-phase cartridges that contain polystyrene-divinylbenzene resin. Cartridges are dried with nitrogen gas, and then sorbed compounds are eluted with dichloromethane-diethyl ether (4:1) and determined by capillary-column gas chromatography/mass spectrometry. Recoveries in reagent-water samples fortified at 4 micrograms per liter averaged 74 percent ? 7 percent relative standard deviation for all method compounds. Initial method detection limits for single-component compounds (excluding hormones and sterols) averaged 0.15 microgram per liter. Samples are preserved by filtration, the addition of 60 grams NaCl, and storage at 4 degrees Celsius. The laboratory has established a sample-holding time (prior to sample extraction) of 14 days from the date of sample collection until a statistically accepted method can be used to determine the effectiveness of these sample-preservation procedures.

  19. Indicator pathogens, organic matter and LAS detergent removal from wastewater by constructed subsurface wetlands

    PubMed Central

    2014-01-01

    Background Constructed wetland is one of the natural methods of municipal and industrial wastewater treatments with low initial costs for construction and operation as well as easy maintenance. The main objective of this study is to determine the values of indicator bacteria removal, organic matter, TSS, ammonia and nitrate affecting the wetland removal efficiency. Results The average concentration of E. coli and total coliform in the input is 1.127?×?1014 and 4.41?×?1014 MPN/100 mL that reached 5.03?×?1012 and 1.13?×?1014 MPN/100 mL by reducing 95.5% and 74.4% in wetland 2. Fecal streptococcus reached from the average 5.88?×?1014 in raw wastewater to 9.69?×?1012 in the output of wetland 2. Wetland 2 could reduce 1.5 logarithmic units of E. coli. The removal efficiency of TSS for the wetlands is 68.87%, 71.4%, 57.3%, and 66% respectively. Conclusions The overall results show that wetlands in which herbs were planted had a high removal efficiency about the indicator pathogens, organic matter, LAS detergent in comparison to a control wetland (without canes) and could improve physicochemical parameters (DO, ammonia, nitrate, electrical conductivity, and pH) of wastewater. PMID:24581277

  20. 40 CFR Table 8 to Subpart G of... - Organic HAP's Subject to the Wastewater Provisions for Process Units at New Sources

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... Wastewater Provisions for Process Units at New Sources 8 Table 8 to Subpart G of Part 63 Protection of... Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 8 Table 8 to Subpart G of Part 63—Organic HAP's Subject to the Wastewater Provisions for Process Units at New Sources Chemical name CAS...

  1. 40 CFR Table 8 to Subpart G of... - Organic HAP's Subject to the Wastewater Provisions for Process Units at New Sources

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Wastewater Provisions for Process Units at New Sources 8 Table 8 to Subpart G of Part 63 Protection of... Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 8 Table 8 to Subpart G of Part 63—Organic HAP's Subject to the Wastewater Provisions for Process Units at New Sources Chemical name CAS...

  2. Removal of organic pollutants by surfactant modified zeolite: comparison between ionizable phenolic compounds and non-ionizable organic compounds.

    PubMed

    Xie, Jie; Meng, Wenna; Wu, Deyi; Zhang, Zhenjia; Kong, Hainan

    2012-09-15

    The aim of this study was to examine the adsorption capability and mechanism of hexadecyltrimethylammonium modified zeolite, which was synthesized from coal fly ash, for the removal of ionizable phenolic compounds (phenol, p-chlorophenol and bisphenol A, with different pK(a)) and non-ionizable organic compounds (aniline, nitrobenzene, and naphthalene, with different hydrophobicity). The obtained zeolite was identified as type Na-P1 (Na(6)Al(6)Si(10)O(32)·12H(2)O, JCPDS code 39-0219), which is classified into the gismondine group with a pore size of 3.1 Ĺ × 4.5 Ĺ [100] and 2.8 Ĺ × 4.8 Ĺ [101]. The adsorption of the two kinds of organic compounds was due to loaded surfactant bilayer because modified zeolite showed great ability for the removal of organic chemicals while little adsorption by zeolite was observed. The isotherm data of ionizable compounds fitted well to the Langmuir model but those of non-ionizable chemicals followed a linear equation. Uptake of ionizable compounds depended greatly on pH, increasing at alkaline pH conditions. In contrary, adsorption of non-ionizable chemicals was essentially the same at all pH levels studied. The adsorption of both kinds of organic compounds correlated well to k(ow) value, suggesting that more hydrophobic organic contaminants are more easily retained by modified zeolite. Based on the different adsorption behavior, the uptake of non-ionizable pollutants was thought to be a single partitioning process into the surfactant bilayer. For ionizable compounds, however, interaction of the phenol group(s) with the positively charged "head" of surfactant additionally functions. PMID:22771348

  3. 75 FR 57412 - Approval and Promulgation of Implementation Plans Alabama: Volatile Organic Compounds

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-09-21

    ...Implementation Plans Alabama: Volatile Organic Compounds AGENCY: Environmental Protection Agency...the definition of ``volatile organic compounds'' (VOCs) found at Alabama Administrative...Specifically, the revision would add two compounds (propylene carbonate and dimethyl...

  4. Impacts of coagulation on the adsorption of organic micropollutants onto powdered activated carbon in treated domestic wastewater.

    PubMed

    Altmann, Johannes; Zietzschmann, Frederik; Geiling, Eva-Linde; Ruhl, Aki Sebastian; Sperlich, Alexander; Jekel, Martin

    2015-04-01

    The application of powdered activated carbon (PAC) as an advanced wastewater treatment step for the removal of organic micropollutants (OMP) necessitates complete separation of the PAC particles, e.g. by coagulation. In this study, potential positive or negative indirect or direct effects of coagulation on the adsorption of OMPs onto PAC in treated wastewater were investigated. Although the concentration of dissolved organic matter (DOM) was significantly reduced by coagulation, the selective removal of mainly larger DOM components such as biopolymers and humic substances did not improve subsequent OMP adsorption onto PAC, demonstrating that coagulation has minor effects on DOM constituents that are relevant for direct competition or pore blocking. The combination of coagulation and adsorption yielded the sum of the individual removals, as adsorption predominantly affected smaller compounds. While the formation of flocs led to visible incorporation of PAC particles, no significant mass transfer limitations impeded the OMP adsorption. As a result, the dosing sequence of coagulant and PAC is not critical for efficient adsorption of OMPs onto PAC. The relationships between adsorptive OMP removal and corresponding reduction of UV absorption at 254 nm (UVA254) as a promising surrogate correlation for the real-time monitoring and PAC adjustment were affected by coagulation, leading to individual correlations depending on the water composition. Correcting for UVA254 reduction by coagulation produces adsorptive UVA254 removal, which correlates highly with OMP removal for different WWTP effluents and varying coagulant doses and can be applied in combined adsorption/coagulation processes to predict OMP removal and control PAC dosing. PMID:25582393

  5. Occurrence, fate and ecotoxicological assessment of pharmaceutically active compounds in wastewater and sludge from wastewater treatment plants in Chongqing, the Three Gorges Reservoir Area.

    PubMed

    Yan, Qing; Gao, Xu; Chen, You-Peng; Peng, Xu-Ya; Zhang, Yi-Xin; Gan, Xiu-Mei; Zi, Cheng-Fang; Guo, Jin-Song

    2014-02-01

    The occurrence, removal and ecotoxicological assessment of 21 pharmaceutically active compounds (PhACs) including antibiotics, analgesics, antiepileptics, antilipidemics and antihypersensitives, were studied at four municipal wastewater treatment plants (WWTP) in Chongqing, the Three Gorges Reservoir Area. Individual treatment unit effluents, as well as primary and secondary sludge, were sampled and analyzed for the selected PhACs to evaluate their biodegradation, persistence and partitioning behaviors. PhACs were identified and quantified using high performance liquid chromatography/tandem mass spectrometry after solid-phase extraction. All the 21 analyzed PhACs were detected in wastewater and the target PhACs except acetaminophen, ibuprofen and gemfibrozil, were also found in sludge. The concentrations of the antibiotics and SVT were comparable to or even higher than those reported in developed countries, while the case of other target PhACs was opposite. The elimination of PhACs except acetaminophen was incomplete and a wide range of elimination efficiencies during the treatment were observed, i.e. from "negative removal" to 99.5%. The removal of PhACs was insignificant in primary and disinfection processes, and was mainly achieved during the biological treatment. Based on the mass balance analysis, biodegradation is believed to be the primary removal mechanism, whereas only about 1.5% of the total mass load of the target PhACs was removed by sorption. Experimentally estimated distribution coefficients (<500 L/kg, with a few exceptions) also indicate that biodegradation/transformation was responsible for the removal of the target PhACs. Ecotoxicological assessment indicated that the environment concentrations of single compounds (including sulfadiazine, sulfamethoxazole, ofloxacin, azithromycin and erythromycin-H2O) in effluent and sludge, as well as the mixture of the 21 detected PhACs in effluent, sludge and receiving water had a significant ecotoxicological risk to algae. Therefore, further control of PhACs in effluent and sludge is required before their discharge and application to prevent their introduction into the environment. PMID:24176710

  6. Key volatile organic compounds emitted from swine nursery house

    NASA Astrophysics Data System (ADS)

    Yao, H. Q.; Choi, H. L.; Zhu, K.; Lee, J. H.

    2011-05-01

    This study was carried out to quantify the concentration and emission levels of key volatile organic compounds (VOCs) - sulfides, indolics, phenolics and volatile fatty acids (VFA) - emitted from swine nursery house, and assess the effect of microclimate (including temperature, relative humidity and air speed) on the key odorous compounds. Samples were collected from the Experimental Farm of Seoul National University in Suwon, South Korea. And the collection took place for four seasons and the sampling time was fixed at 10:30 in the morning. The application of one-way ANOVA and Bonferroni t analyses revealed that, most of the odorous compound concentrations, such as dimethyl sulfide (DMS), dimethyl disulfide (DMDS), indole, p-cresol and all the volatile fatty acids were lowest during the summer ( P < 0.01). Meanwhile, negative correlations were observed between temperature and odorants, as well as air speed and odorants. A possible reason was that high ventilation transferred most of the odors out of the house during the summer. From the whole year data, non-linear multiple regressions were conducted and the equations were proposed depending upon the relationships between microclimate parameters and odorous compounds. The equations were applied in hope of easily calculating the concentrations of the odorous compounds in the commercial farms. The results obtained in this study should be used for reducing the volatile organic compounds by controlling microclimate parameters and also could be helpful in setting a guideline for good management practices in nursery house.

  7. Analysis of Organic Compounds in Mars Analog Samples

    NASA Technical Reports Server (NTRS)

    Mahaffy, P. R.; Brinckerhoff, W. B.; Buch, A.; Cabane, M.; Coll, P.; Demick, J.; Glavin, D. P.

    2004-01-01

    The detailed characterization of organic compounds that might be preserved in rocks, ices, or sedimentary layers on Mars would be a significant step toward resolving the question of the habitability and potential for life on that planet. The fact that the Viking gas chromatograph mass spectrometer (GCMS) did not detect organic compounds should not discourage further investigations since (a) an oxidizing environment in the near surface fines analyzed by Viking is likely to have destroyed many reduced carbon species; (b) there are classes of refractory or partially oxidized species such as carboxylic acids that would not have been detected by the Viking GCMS; and (c) the Viking landing sites are not representative of Mars overall. These factors motivate the development of advanced in situ analytical protocols to carry out a comprehensive survey of organic compounds in martian regolith, ices, and rocks. We combine pyrolysis GCMS for analysis of volatile species, chemical derivatization for transformation of less volatile organics, and laser desorption mass spectrometry (LDMS) for analysis of elements and more refractory, higher-mass organics. To evaluate this approach and enable a comparison with other measurement techniques we analyze organics in Mars simulant samples.

  8. Volatile organic compounds of Angelica gigas Nakai, Korean medicinal herb.

    PubMed

    Seo, Hye-Young; Yang, Su-Hyeong; Shim, Sung-Lye; No, Ki-Mi; Park, Kyung-Su; Song, Ki-Dong; Kim, Kyong-Su

    2007-03-01

    The study was performed to find out the profile of volatile flavor components from the aromatic medicinal plant, Angelica gigas Nakai. The volatile organic compounds of A. gigas Nakai were extracted by simultaneous steam distillation and extraction (SDE) method, and identified by gas chromatograph/mass spectrometric (GC/MS) analysis. A total of 116 compounds, including 40 hydrocarbons, 37 alcohols, 15 esters, 12 aldehydes, 7 ketones, and 5 miscellaneous were identified and quantified. Among them, 75 volatile organic compounds were detected which make up 90.52% of total volatile content. alpha-Pinene was detected as the prime volatile component which accounted for 30.89% of total volatile content and 2,4,6-trimethyl heptane, camphene, alpha-limonene, beta-eudesmol, vervenol, alpha-murrolene, and sphatulenol were detected as the major components of A. gigas Nakai. PMID:17365718

  9. Biotransformations of organic compounds mediated by cultures of Aspergillus niger.

    PubMed

    Parshikov, Igor A; Woodling, Kellie A; Sutherland, John B

    2015-09-01

    Many different organic compounds may be converted by microbial biotransformation to high-value products for the chemical and pharmaceutical industries. This review summarizes the use of strains of Aspergillus niger, a well-known filamentous fungus used in numerous biotechnological processes, for biochemical transformations of organic compounds. The substrates transformed include monocyclic, bicyclic, and polycyclic aromatic hydrocarbons; azaarenes, epoxides, chlorinated hydrocarbons, and other aliphatic and aromatic compounds. The types of reactions performed by A. niger, although not unique to this species, are extremely diverse. They include hydroxylation, oxidation of various functional groups, reduction of double bonds, demethylation, sulfation, epoxide hydrolysis, dechlorination, ring cleavage, and conjugation. Some of the products may be useful as new investigational drugs or chemical intermediates. PMID:26162670

  10. Organic constituents in sour condensates from shale-oil and petroleum-crude runs at Sohio's Toledo refinery: identification and wastewater-control-technology considerations

    SciTech Connect

    Wingender, R J; Harrison, W; Raphaelian, L A

    1981-02-01

    Samples of sour condensate generated from the continuous processing of both crude shale oil and petroleum crude were collected and extracted with methylene chloride. The extracts were analyzed using capillary-column gas chromatography/mass spectrometry at Argonne National Laboratory and Radian Corporation. Qualitatively, the predominant types of organic compounds present in the shale-oil sour condensate were pyridines and anilines; semiquantitatively, these compounds were present at a concentration of 5.7 ppM, or about 78% of the total concentration of components detected. In contrast, straight-chain alkanes were the predominant types of compounds found in the sour condensate produced during isocracking of conventional crude oil. The approximate concentration of straight-chain alkanes, 8.3 ppM, and of other branched and/or unsaturated hydrocarbons, 6.8 ppM, amounted to 88% of the total concentration of components detected in the sour condensate from the petroleum-crude run. Nitrogen compounds in the shale-oil sour condensate may necessitate alterations of the sour water and refinery wastewater-treatment facilities to provide for organics degradation and to accommodate the potentially greater ammonia loadings. This would include use of larger amounts of caustic to enhance ammonia removal by steam stripping. Possible problems associated with biological removal of organic-nitrogen compounds should be investigated in future experimental shale-oil refining runs.

  11. Modeling emissions of volatile organic compounds from silage

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Photochemical smog is a major air pollution problem and a significant cause of premature death in the U.S. Smog forms in the presence of volatile organic compounds (VOCs), which are emitted primarily from industry and motor vehicles in the U.S. However, dairy farms may be an important source in so...

  12. Influence of volatile organic compounds on Fusarium graminearum mycotoxin production

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Volatile organic compounds (VOCs) are involved in a diverse range of ecological interactions. Due to their low molecular weight, lipophilic nature, and high vapor pressure at ambient temperatures, they can serve as airborne signaling molecules that are capable of mediating inter and intraspecies com...

  13. OXYGENATED ORGANIC COMPOUND CONCENTRATIONS NEAR A ROADWAY IN LITHUANIA, SSR

    EPA Science Inventory

    During the period June 1 to June 9, 1989, aldehyde and other oxygenated organic compound concentrations were examined at sites 3, 10, and 80 meters northeast of the Vilnius-Kaunas highway in Lithuania, SSR by collecting 120 liter (1 L/min for 120 min) samples on 2,4-dinitrophenyl...

  14. PHOTOTHERMAL DESTRUCTION OF THE VAPOR OF ORGANIC COMPOUNDS

    EPA Science Inventory

    The results of thermal and photothermal destruction of the vapors of organic compounds were compared by conducting tests in a photothermal detoxification unit. enon are lamp was used as the irradiation source. he tests were conducted on trichlorethylene (TCE), 1,2-dichlorobenzene...

  15. FIELD-DEPLOYABLE MONITORS FOR VOLATILE ORGANIC COMPOUNDS IN AIR

    EPA Science Inventory

    Volatile organic compounds in ambient air are usually estimated by trapping them from air or collecting whole air samples and returning them to a laboratory for analysis by gas chromatography using selective detection. ata do not appear for several days, during which sample integ...

  16. Volatile Organic Compounds in Untreated Ambient Groundwater of

    E-print Network

    Volatile Organic Compounds in Untreated Ambient Groundwater of the United States, 1985-1995 P A U L, ambient groundwater of the conterminous United States was conducted based on samples collected from 2948-chloropropane, which had a reporting level of 1.0 µg/L. Because ambient groundwater was targeted, areas of known

  17. MEASUREMENT OF ORGANIC COMPOUND EMISSIONS USING SMALL TEST CHAMBERS

    EPA Science Inventory

    Organic compounds emitted from a variety of indoor materials have been measured using small (166 L) environmental test chambers. The paper discusses: a) factors to be considered in small chamber testing; b) parameters to be controlled; c) the types of results obtained. The follow...

  18. Volatile organic compound emissions from dairy facilities in central California

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Emissions of volatile organic compounds (VOCs) from dairy facilities are thought to be an important contributor to high ozone levels in central California, but emissions inventories from these sources contain significant uncertainties. In this work, VOC emissions were measured at two central Califor...

  19. Qualitative analysis of volatile organic compounds on biochar

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Qualitative identification of sorbed volatile organic compounds (VOCs) on biochar was conducted by headspace thermal desorption coupled to capillary gas chromatographic-mass spectrometry. VOCs may have a mechanistic role influencing plant and microbial responses to biochar amendments, since VOCs ca...

  20. 40 CFR 60.722 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 7 2014-07-01 2014-07-01 false Standards for volatile organic compounds. 60.722 Section 60.722 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) STANDARDS OF PERFORMANCE FOR NEW STATIONARY SOURCES Standards of Performance for Industrial Surface Coating: Surface Coating...

  1. 40 CFR 60.722 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 7 2012-07-01 2012-07-01 false Standards for volatile organic compounds. 60.722 Section 60.722 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) STANDARDS OF PERFORMANCE FOR NEW STATIONARY SOURCES Standards of Performance for Industrial Surface Coating: Surface Coating...

  2. 40 CFR 60.722 - Standards for volatile organic compounds.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 7 2013-07-01 2013-07-01 false Standards for volatile organic compounds. 60.722 Section 60.722 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) STANDARDS OF PERFORMANCE FOR NEW STATIONARY SOURCES Standards of Performance for Industrial Surface Coating: Surface Coating...

  3. The Survival of Meteorite Organic Compounds with Increasing Impact Pressure

    NASA Technical Reports Server (NTRS)

    Cooper, George; Horz, Friedrich; Oleary, Alanna; Chang, Sherwood; DeVincenzi, Donald L. (Technical Monitor)

    2000-01-01

    The majority of carbonaceous meteorites studied today are thought to originate in the asteroid belt. Impacts among asteroidal objects generate heat and pressure that may have altered or destroyed pre-existing organic matter in both targets and projectiles to a greater or lesser degree depending upon impact velocities. Very little is known about the shock related chemical evolution of organic matter relevant to this stage of the cosmic history of biogenic elements and compounds. The present work continues our study of the effects of shock impacts on selected classes of organic compounds utilizing laboratory shock facilities. Our approach was to subject mixtures of organic compounds, embedded in a matrix of the Murchison meteorite, to a simulated hypervelocity impact. The molecular compositions of products were then analyzed to determine the degree of survival of the original compounds. Insofar as results associated with velocities < 8 km/sec may be relevant to impacts on planetary surfaces (e.g., oblique impacts, impacts on small outer planet satellites) or grain-grain collisions in the interstellar medium, then our experiments will be applicable to these environments as well.

  4. DESTRUCTION OF VOLATILE ORGANIC COMPOUNDS VIA CATALYTIC INCINERATION (JOURNAL VERSION)

    EPA Science Inventory

    The paper gives results of an investigation of the effect of catalytic incinerator design and operation on the destruction of specific volatile organic compounds (VOCs), both singly and in mixtures. A range of operating and design parameters were tested on a wide variety of compo...

  5. FIELD EXPERIENCE WITH FOUR PORTABLE VOC (VOLATILE ORGANIC COMPOUND) MONITORS

    EPA Science Inventory

    This report discusses the field operation problems associated with use of four portable volatile organic compound (VOC) detection instruments in conducting Reference Method 21 VOC screenings. The report presents the results of the field trials and summarizes the ease of use of ea...

  6. VOC (VOLATILE ORGANIC COMPOUND) FUGITIVE EMISSION PREDICTIVE MODEL - USER'S GUIDE

    EPA Science Inventory

    The report discusses a mathematical model that can be used to evaluate the effectiveness of various leak detection and repair (LDAR) programs on controlling volatile organic compound (VOC) fugitive emissions from chemical, petroleum, and other process units. The report also descr...

  7. VOLATILE ORGANIC COMPOUND MODEL (VERSION 1.8) (FOR MICROCOMPUTERS)

    EPA Science Inventory

    Future emissions of volatile organic compounds (VOCs) and costs of their control can be estimated by applying growth factors, emission constraints, control cost functions, and capacity retirement rates to the base line estimates of VOC emissions and industrial VOC source capacity...

  8. SORPTION OF IONIZABLE ORGANIC COMPOUNDS TO SEDIMENTS AND SOILS

    EPA Science Inventory

    The sorption of ionizable organic compounds to sediments and saturated soils is examined. he sorption of pentachlorophenol to two sediment silt-clay fractions as a function of pH is described. Sorption of both the neutral and the ionic species was shown to occur; results were qua...

  9. AERATION TO REMOVE VOLATILE ORGANIC COMPOUNDS FROM GROUND WATER

    EPA Science Inventory

    The interim report presents general information on the use of aeration to remove volatile organic compounds from drinking water for public health reasons. The report illustrates the types of aerators, shows where they are being used, presents a means of estimating aeration perfor...

  10. MICROBIAL VOLATILE ORGANIC COMPOUND EMISSION RATES AND EXPOSURE MODEL

    EPA Science Inventory

    This paper presents the results from a study that examined microbial volatile organic compound (MVOC) emissions from six fungi and one bacterial species (Streptomyces spp.) commonly found in indoor environments. Data are presented on peak emission rates from inoculated agar plate...

  11. Modeling emissions of volatile organic compounds from silage

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Volatile organic compounds (VOCs), necessary reactants for photochemical smog formation, are emitted from numerous sources. Limited available data suggest that dairy farms emit VOCs with cattle feed, primarily silage, being the primary source. Process-based models of VOC transfer within and from si...

  12. Measuring Emissions of Volatile Organic Compounds from Silage

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Volatile organic compound (VOC) emissions are considered to be important precursors to smog and ozone production. An experimental protocol was developed to obtain undisturbed silage samples from silage storages. Samples were placed in a wind tunnel where temperature, humidity, and air flow were cont...

  13. LEAVES AS INDICATORS OF EXPOSURE TO AIRBORNE VOLATILE ORGANIC COMPOUNDS

    EPA Science Inventory

    The concentration of volatile organic compounds (VOCs) in leaves is primarily a product of airborne exposures and dependent upon bioconcentration factors and release rates. The bioconcentration factors for VOCs in grass are found to be related to their partitioning between octan...

  14. 40 CFR 60.442 - Standard for volatile organic compounds.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for volatile organic compounds. 60.442 Section 60.442 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Pressure Sensitive Tape and Label Surface Coating Operations § 60.442 Standard for volatile...

  15. 40 CFR 60.442 - Standard for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 6 2011-07-01 2011-07-01 false Standard for volatile organic compounds. 60.442 Section 60.442 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Pressure Sensitive Tape and Label Surface Coating Operations § 60.442 Standard for volatile...

  16. Bioprofiling of Surface/Wastewater and Bioquantitation of Discovered Endocrine-Active Compounds by Streamlined Direct Bioautography.

    PubMed

    Klingelhöfer, Ines; Morlock, Gertrud E

    2015-11-01

    A direct bioautography has been used for the simultaneous determination of four estrogens [estrone (E1), 17?-estradiol (E2), estriol (E3), and 17?-ethinylestradiol (EE2)] and two xenoestrogens [bisphenol A (BPA) and 4-n-nonyl-phenol (NP)] in surface water and wastewater samples from a sewage treatment plant. After either direct application or a liquid-liquid extraction of the water samples, the qualitative and quantitative detection of estrogen-effective compounds was performed with a planar yeast estrogen screen. The limits of detection were different for each compound, due to the specific receptor binding of individual (xeno)estrogens (1 ng/L to 15 ?g/L). The mean recovery rate for all six substances at this ultratrace level was 88% [mean percent relative standard deviation (%RSD) of 17%, n = 3]. Over the whole procedure, precisions of three estrogens discovered in a wastewater sample were below 17%, n = 3. The identification of the detected bioactive compounds was performed by high-performance thin-layer chromatography-electrospray ionization mass spectrometry (HPTLC-ESI-MS) via the elution-head-based TLC-MS Interface. Whereas the estrogens E1 and E2 could always be detected in the influent of the treatment plant, E3 was detected occasionally. The concentrations of E1 and E2 ranged from 3 to 50 ng/L, and for E3 from 98 to 210 ng/L. EE2, BPA, and NP could not be detected at the given LOD. In every second surface water sample, E1 and E2 were detected, but not E3, EE2, BPA, and NP. PMID:26447851

  17. A novel biosensor based on Lactobacillus acidophilus for determination of phenolic compounds in milk products and wastewater.

    PubMed

    Sagiroglu, Ayten; Paluzar, Hatice; Ozcan, Hakki Mevlut; Okten, Suzan; Sen, Burhan

    2011-01-01

    Different branches of industry need to use phenolic compounds (PCs) in their production, so determination of PCs sensitively, accurately, rapidly, and economically is very important. For the sensitive determination of PCs, some biosensors based on pure polyphenol oxidase, plant tissue and microorganisms were developed before. But there has been no study to develop a microbial phenolic compounds biosensor based on Lactobacillus species, which contain polyphenol oxidase enzyme. In this study, we used different forms of Lactobacillus species as enzyme sources of biosensor and compared biosensor performances of these forms for determination of PCs. For this purpose, we used lyophilized Lactobacillus cells (containing L. bulgaricus, L. acidophilus, Streptococcus thermophilus), pure L. acidophilus, pure L. bulgaricus, and L. acidophilus- and L. bulgaricus adapted to catechol in Lactobacilli MRS Broth. The most suitable form was determined and optimization studies of the biosensor were carried out by using this form. For preparing the bioactive layer of the biosensor, the Lactobacillus cells were immobilized in gelatin by using glutaraldehyde. In the study, we used catechol as a substrate. Phenolic compound determination is based on the assay of the differences on the respiration activity of the cells on the oxygen meter in the absence and the presence of catechol. The microbial biosensor response depends directly on catechol concentration between 0.5 and 5.0 mM with 18 min response time. In the optimization studies of the microbial biosensor the most suitable microorganism amount was found to be 10 mg, and also phosphate buffer (pH 8.0; 50 mM) and 37.5 °C were obtained as the optimum working conditions. In the characterization studies of the microbial biosensor some parameters such as substrate specificity on the biosensor response and operational and storage stability were examine. Furthermore, the determination of PC levels in synthetic wastewater, industrial wastewater, and milk products was investigated by using the developed biosensor under optimum conditions. PMID:21967334

  18. Post-treatment of biologically treated wastewater containing organic contaminants using a sequence of H2O2 based advanced oxidation processes: photolysis and catalytic wet oxidation.

    PubMed

    Rueda-Márquez, J J; Sillanpää, M; Pocostales, P; Acevedo, A; Manzano, M A

    2015-03-15

    In this paper the feasibility of a multi-barrier treatment (MBT) for the regeneration of synthetic industrial wastewater (SIWW) was evaluated. Industrial pollutants (orange II, phenol, 4-chlorophenol and phenanthrene) were added to the effluent of municipal wastewater treatment plant. The proposed MBT begins with a microfiltration membrane pretreatment (MF), followed by hydrogen peroxide photolysis (H2O2/UVC) and finishing, as a polishing step, with catalytic wet peroxide oxidation (CWPO) using granular activated carbon (GAC) at ambient conditions. During the microfiltration step (0.7 ?m) the decrease of suspended solids concentration, turbidity and Escherichia coli in treated water were 88, 94 and 99%, respectively. Also, the effluent's transmittance (254 nm) was increased by 14.7%. Removal of more than 99.9% of all added pollutants, mineralization of 63% of organic compounds and complete disinfection of total coliforms were reached during the H2O2/UVC treatment step (H2O2:TOC w/w ratio = 5 and an UVC average dose accumulated by wastewater 8.80 WUVC s cm(-2)). The power and efficiency of the lamp, the water transmittance and photoreactor geometry are taken into account and a new equation to estimate the accumulated dose in water is suggested. Remaining organic pollutants with a higher oxidation state of carbon atoms (+0.47) and toxic concentration of residual H2O2 were present in the effluent of the H2O2/UVC process. After 2.3 min of contact time with GAC at CWPO step, 90 and 100% of total organic carbon and residual H2O2 were removed, respectively. Also, the wastewater toxicity was studied using Vibrio fischeri and Sparus aurata larvae. The MBT operational and maintenance costs (O&M) was estimated to be 0.59 € m(-3). PMID:25600300

  19. Emission of volatile organic compounds from silage: compounds, sources, and implications

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Silage, fermented cattle feed, has recently been identified as a significant source of volatile organic compounds (VOCs) emitted to the atmosphere. A small number of studies have measured VOC emission from silage, but not enough is known about the processes involved to accurately quantify emission r...

  20. Determination of fluorine in organic compounds: Microcombustion method

    USGS Publications Warehouse

    Clark, H.S.

    1951-01-01

    A reliable and widely applicable means of determining fluorine in organic compounds has long been needed. Increased interest in this field of research in recent years has intensified the need. Fluorine in organic combinations may be determined by combustion at 900?? C. in a quartz tube with a platinum catalyst, followed by an acid-base titration of the combustion products. Certain necessary precautions and known limitations are discussed in some detail. Milligram samples suffice, and the accuracy of the method is about that usually associated with the other halogen determinations. Use of this method has facilitated the work upon organic fluorine compounds in this laboratory and it should prove to be equally valuable to others.

  1. Molecular Donor-Acceptor Compounds as Prospective Organic Electronics Materials

    NASA Astrophysics Data System (ADS)

    Horiuchi, Sachio; Hasegawa, Tatsuo; Tokura, Yoshinori

    2006-05-01

    The ?-electronic functionalities of molecular donor (D)-acceptor (A) compounds have been attracting subjects for the solid state science as well as for the prospective technological exploitation in organic electronics. In this review, it is shown that the novel neutral-ionic valence instability in the charge-transfer (CT) complexes is closely related to valuable electric properties such as the current-induced resistance switching, quantum phase transition, gigantic dielectric response, and relaxor ferroelectricity. Furthermore, the displacive-type ferroelectricity has recently been developed on the DA combinations in the hydrogen-bonded co-crystals. It is also discussed that the intermolecular CT mechanism in the molecular DA compounds is promising to advance the potential of organic field-effect transistors (FETs) that are envisioned as key components in future organic electronics.

  2. 40 CFR 60.112b - Standard for volatile organic compounds (VOC).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...2014-07-01 false Standard for volatile organic compounds (VOC). 60.112b Section... Standards of Performance for Volatile Organic Liquid Storage Vessels (Including Petroleum... § 60.112b Standard for volatile organic compounds (VOC). (a) The...

  3. 40 CFR 60.112b - Standard for volatile organic compounds (VOC).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...2013-07-01 false Standard for volatile organic compounds (VOC). 60.112b Section... Standards of Performance for Volatile Organic Liquid Storage Vessels (Including Petroleum... § 60.112b Standard for volatile organic compounds (VOC). (a) The...

  4. 40 CFR 60.112b - Standard for volatile organic compounds (VOC).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...2012-07-01 false Standard for volatile organic compounds (VOC). 60.112b Section... Standards of Performance for Volatile Organic Liquid Storage Vessels (Including Petroleum... § 60.112b Standard for volatile organic compounds (VOC). (a) The...

  5. Dynamics of soil organic carbon and microbial activity in treated wastewater irrigated agricultural soils along soil profiles

    NASA Astrophysics Data System (ADS)

    Jüschke, Elisabeth; Marschner, Bernd; Chen, Yona; Tarchitzky, Jorge

    2010-05-01

    Treated wastewater (TWW) is an important source for irrigation water in arid and semiarid regions and already serves as an important water source in Jordan, the Palestinian Territories and Israel. Reclaimed water still contains organic matter (OM) and various compounds that may effect microbial activity and soil quality (Feigin et al. 1991). Natural soil organic carbon (SOC) may be altered by interactions between these compounds and the soil microorganisms. This study evaluates the effects of TWW irrigation on the quality, dynamics and microbial transformations of natural SOC. Priming effects (PE) and SOC mineralization were determined to estimate the influence of TWW irrigation on SOC along soil profiles of agricultural soils in Israel and the Westbank. The used soil material derived from three different sampling sites allocated in Israel and The Palestinian Authority. Soil samples were taken always from TWW irrigated sites and control fields from 6 different depths (0-10, 10-20, 20-30, 30-50, 50-70, 70-100 cm). Soil carbon content and microbiological parameters (microbial biomass, microbial activities and enzyme activities) were investigated. In several sites, subsoils (50-160 cm) from TWW irrigated plots were depleted in soil organic matter with the largest differences occurring in sites with the longest TWW irrigation history. Laboratory incubation experiments with additions of 14C-labelled compounds to the soils showed that microbial activity in freshwater irrigated soils was much more stimulated by sugars or amino acids than in TWW irrigated soils. The lack of such "priming effects" (Hamer & Marschner 2005) in the TWW irrigated soils indicates that here the microorganisms are already operating at their optimal metabolic activity due to the continuous substrate inputs with soluble organic compounds from the TWW. The fact that PE are triggered continuously due to TWW irrigation may result in a decrease of SOC over long term irrigation. Already now this could be detected at some agricultural fields by SOC measurements (Jüschke 2009). Therefore attention has to be drawn especially on the carbon content and quality of the used TWW for irrigation purposes.

  6. Group extraction of organic compounds present in liquid samples

    NASA Technical Reports Server (NTRS)

    Jahnsen, Vilhelm J. (Inventor)

    1976-01-01

    An extraction device is disclosed comprising a tube containing a substantially inert, chemically non-reactive packing material with a large surface area to volume ratio. A sample which consists of organic compounds dissolved in a liquid, is introduced into the tube. As the sample passes through the packing material it spreads over the material's large surface area to form a thin liquid film which is held on the packing material in a stationary state. A particular group or family of compounds is extractable from the sample by passing a particular solvent system consisting of a solvent and selected reagents through the packing material. The reagents cause optimum conditions to exist for the compounds of the particular family to pass through the phase boundary between the sample liquid and the solvent of the solvent system. Thus, the compounds of the particular family are separated from the sample liquid and become dissolved in the solvent of the solvent system. The particular family of compounds dissolved in the solvent, representing an extract, exits the tube together with the solvent through the tube's nozzle, while the rest of the sample remains on the packing material in a stationary state. Subsequently, a different solvent system may be passed through the packing material to extract another family of compounds from the remaining sample on the packing material.

  7. A Review of the Tissue Residue Approach for Organic and Organometallic Compounds in Aquatic Organisms

    EPA Science Inventory

    This paper reviews the tissue residue approach (TRA) for toxicity assessment as it applies to organic chemicals and some organometallic compounds (tin, mercury, and lead). Specific emphasis was placed on evaluating key factors that influence interpretation of critical body resid...

  8. DISTRIBUTION OF HYDROPHOBIC IONOGENIC ORGANIC COMPOUNDS BETWEEN OCTANOL AND WATER: ORGANIC ACIDS

    EPA Science Inventory

    The octanol-water distributions of 10 environmentally significant organic acid compounds were determined as a function of aqueous-phase salt concentration (0.05-0.2 M LiCl, NaCl, KCl, CaCl2, or MgCl2) and pH. he compounds were pentachlorophenol 2,3,4,5-tetrachlorophenol, (2,4,5-t...

  9. 40 CFR Table 34 to Subpart G of... - Fraction Measured (Fm) and Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 9 2010-07-01 2010-07-01 false Fraction Measured (Fm) and Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams 34 Table 34 to Subpart G of Part 63 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR...

  10. 40 CFR Table 34 to Subpart G of... - Fraction Measured (Fm) and Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 9 2011-07-01 2011-07-01 false Fraction Measured (Fm) and Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams 34 Table 34 to Subpart G of Part 63 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR...

  11. 40 CFR Table 34 to Subpart G of... - Fraction Measured (Fm) and Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 10 2013-07-01 2013-07-01 false Fraction Measured (Fm) and Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams 34 Table 34 to Subpart G of Part 63 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR...

  12. 40 CFR Table 34 to Subpart G of... - Fraction Measured (Fm) and Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 10 2012-07-01 2012-07-01 false Fraction Measured (Fm) and Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams 34 Table 34 to Subpart G of Part 63 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR...

  13. 40 CFR Table 34 to Subpart G of... - Fraction Measured (Fm) and Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 10 2014-07-01 2014-07-01 false Fraction Measured (Fm) and Fraction Emitted (Fe) For HAP Compounds in Wastewater Streams 34 Table 34 to Subpart G of Part 63 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR...

  14. Identification and Quantification of Volatile Organic Compounds at a Dairy

    NASA Astrophysics Data System (ADS)

    Filipy, J.; Mount, G.; Westberg, H.; Rumburg, B.

    2003-12-01

    Livestock operations in the United States are an escalating environmental concern. The increasing density of livestock within a farm results in an increased emission of odorous gases, which have gained considerable attention by the public in recent years (National Research Council (NRC), 2002). Odorous compounds such as ammonia (NH3), volatile organic compounds (VOC's), and hydrogen sulfide (H2S) were reported to have a major effect on the quality of life of local residents living near livestock facilities (NRC, 2002). There has been little data collected related to identification and quantification of gaseous compounds collected from open stall dairy operations in the United States. The research to be presented identifies and quantifies VOCs produced from a dairy operation that contribute to odor and other air quality problems. Many different VOCs were identified in the air downwind of an open lactating cow stall area and near a waste lagoon at the Washington State University dairy using Gas Chromatography Mass Spectroscopy (GC-MS) analysis techniques. Identified compounds were very diverse and included many alcohols, aldehydes, amines, aromatics, esters, ethers, a fixed gas, halogenated hydrocarbons, hydrocarbons, ketones, other nitrogen containing compounds, sulfur containing compounds, and terpenes. The VOCs directly associated with cattle waste were dependent on ambient temperature, with the highest emissions produced during the summer months. Low to moderate wind speeds were ideal for VOC collection. Concentrations of quantified compounds were mostly below odor detection thresholds found in the literature, however the combined odor magnitude of the large number of compounds detected was most likely above any minimum detection threshold.

  15. Method development for measuring biodegradable organic carbon in reclaimed and treated wastewaters

    SciTech Connect

    Khan, E.; Babcock, R.W. Jr.; Suffet, I.H.; Stenstrom, M.K.

    1998-07-01

    Analyses that measure oxygen demand, such as biochemical oxygen demand (BOD) and chemical oxygen demand (COD) analyses, have long been used as indicators of contamination and wastewater treatment plant efficiency. They measure the tendency of pollutants to react with oxygen, which is generally a good indicator of the stability or level of treatment. Both parameters include reactions with organic as well as inorganic substances and suffer from a lack of precision and accuracy at low concentrations, which are becoming increasingly more important. Biodegradable dissolved organic carbon (BDOC) analysis is a relatively new procedure that has advantages over both BOD and COD analyses, including insensitivity to inorganic oxidations. A modified BDOC procedure was developed to characterize the performance of advanced treatment methods, such as those used in municipal water reclamation and secondary-treated wastewaters, where moderately low dissolved organic carbon concentrations (4 to 15 mg/L) are routinely encountered. The development of the modified BDOC procedure was based on a combination of the existing batch BDOC protocol and BOD techniques. Various aspects and incubation conditions were investigated to finalize the procedure. Nitrification does not interfere with the procedure. It is possible to simultaneously determine the soluble BOD (SBOD) under certain conditions. The procedure has reduced variability and increased precision as compared to BOD and COD analyses.

  16. Natural organic compounds as tracers for biomass combustion in aerosols

    SciTech Connect

    Simoneit, B.R.T. |; Abas, M.R. bin |; Cass, G.R. |; Rogge, W.F. |; Mazurek, M.A.; Standley, L.J.; Hildemann, L.M.

    1995-08-01

    Biomass combustion is an important primary source of carbonaceous particles in the global atmosphere. Although various molecular markers have already been proposed for this process, additional specific organic tracers need to be characterized. The injection of natural product organic tracers to smoke occurs primarily by direct volatilization/steam stripping and by thermal alteration based on combustion temperature. The degree of alteration increases as the burn temperature rises and the moisture content of the fuel decreases. Although the molecular composition of organic matter in smoke particles is highly variable, the molecular structures of the tracers are generally source specific. The homologous compound series and biomarkers present in smoke particles are derived directly from plant wax, gum and resin by volatilization and secondarily from pyrolysis of biopolymers, wax, gum and resin. The complexity of the organic components of smoke aerosol is illustrated with examples from controlled burns of temperate and tropical biomass fuels. Burning of biomass from temperate regions (i.e., conifers) yields characteristic tracers from diterpenoids as well as phenolics and other oxygenated species, which are recognizable in urban airsheds. The major organic components of smoke particles from tropical biomass are straight-chain, aliphatic and oxygenated compounds and triterpenoids. The precursor-to-product approach of organic geochemistry can be applied successfully to provide tracers for studying smoke plume chemistry and dispersion.

  17. Transport of chemical and microbial compounds from known wastewater discharges: Potential for use as indicators of human fecal contamination

    USGS Publications Warehouse

    Glassmeyer, S.T.; Furlong, E.T.; Kolpin, D.W.; Cahill, J.D.; Zaugg, S.D.; Werner, S.L.; Meyer, M.T.; Kryak, D.D.

    2005-01-01

    The quality of drinking and recreational water is currently (2005) determined using indicator bacteria. However, the culture tests used to analyze forthese bacteria require a long time to complete and do not discriminate between human and animal fecal material sources. One complementary approach is to use chemicals found in human wastewater, which would have the advantages of (1) potentially shorter analysis times than the bacterial culture tests and (2) being selected for human-source specificity. At 10 locations, water samples were collected upstream and at two successive points downstream from a wastewaster treatment plant (WWTP); a treated effluent sample was also collected at each WWTP. This sampling plan was used to determine the persistence of a chemically diverse suite of emerging contaminants in streams. Samples were also collected at two reference locations assumed to have minimal human impacts. Of the 110 chemical analytes investigated in this project, 78 were detected at least once. The number of compounds in a given sample ranged from 3 at a reference location to 50 in a WWTP effluent sample. The total analyte load at each location varied from 0.018 ??g/L at the reference location to 97.7 ??g/L in a separate WWTP effluent sample. Although most of the compound concentrations were in the range of 0.01-1.0 ??g/L, in some samples, individual concentrations were in the range of 5-38 ??g/L The concentrations of the majority of the chemicals present in the samples generally followed the expected trend: they were either nonexistent or at trace levels in the upstream samples, had their maximum concentrations in the WWTP effluent samples, and then declined in the two downstream samples. This research suggests that selected chemicals are useful as tracers of human wastewater discharge. ?? 2005 American Chemical Society.

  18. Transport of chemical and microbial compounds from known wastewater discharges: potential for use as indicators of human fecal contamination.

    PubMed

    Glassmeyer, Susan T; Furlong, Edward T; Kolpin, Dana W; Cahill, Jeffery D; Zaugg, Steven D; Werner, Stephen L; Meyer, Michael T; Kryak, David D

    2005-07-15

    The quality of drinking and recreational water is currently (2005) determined using indicator bacteria. However, the culture tests used to analyze forthese bacteria require a long time to complete and do not discriminate between human and animal fecal material sources. One complementary approach is to use chemicals found in human wastewater, which would have the advantages of (1) potentially shorter analysis times than the bacterial culture tests and (2) being selected for human-source specificity. At 10 locations, water samples were collected upstream and at two successive points downstream from a wastewaster treatment plant (WWTP); a treated effluent sample was also collected at each WWTP. This sampling plan was used to determine the persistence of a chemically diverse suite of emerging contaminants in streams. Samples were also collected at two reference locations assumed to have minimal human impacts. Of the 110 chemical analytes investigated in this project, 78 were detected at least once. The number of compounds in a given sample ranged from 3 at a reference location to 50 in a WWTP effluent sample. The total analyte load at each location varied from 0.018 microg/L at the reference location to 97.7 microg/L in a separate WWTP effluent sample. Although most of the compound concentrations were in the range of 0.01-1.0 microg/L, in some samples, individual concentrations were in the range of 5-38 microg/L. The concentrations of the majority of the chemicals present in the samples generally followed the expected trend: they were either nonexistent or at trace levels in the upstream samples, had their maximum concentrations in the WWTP effluent samples, and then declined in the two downstream samples. This research suggests that selected chemicals are useful as tracers of human wastewater discharge. PMID:16082943

  19. Organic carbon, influent microbial diversity and temperature strongly influence algal diversity and biomass in raceway ponds treating raw municipal wastewater.

    PubMed

    Cho, Dae-Hyun; Ramanan, Rishiram; Heo, Jina; Kang, Zion; Kim, Byung-Hyuk; Ahn, Chi-Yong; Oh, Hee-Mock; Kim, Hee-Sik

    2015-09-01

    Algae based wastewater treatment coupled to biofuel production has financial benefits and practical difficulties. This study evaluated the factors influencing diversity and growth of indigenous algal consortium cultivated on untreated municipal wastewater in a high rate algal pond (HRAP) for a period of 1 year using multivariate statistics. Diversity analyses revealed the presence of Chlorophyta, Cyanophyta and Bacillariophyta. Dominant microalgal genera by biovolume in various seasons were Scenedesmus sp., Microcystis sp., and Chlorella sp. Scenedesmus sp., persisted throughout the year but none of three strains co-dominated with the other. The most significant factors affecting genus dominance were temperature, inflow cyanophyta and organic carbon concentration. Cyanophyta concentration affected microalgal biomass and diversity, whereas temperature impacted biomass. Preferred diversity of microalgae is not sustained in wastewater systems but is obligatory for biofuel production. This study serves as a guideline to sustain desired microalgal consortium in wastewater treatment plants for biofuel production. PMID:25746593

  20. Removal of organic pollutants in industrial wastewater with an integrated system of copper electrocoagulation and electrogenerated H?O?.

    PubMed

    Barrera-Díaz, Carlos; Frontana-Uribe, Bernado; Bilyeu, Bryan

    2014-06-01

    The effectiveness of organics removal of an integrated electrochemical process, namely, electrocoagulation with copper ions followed by the use of electrogenerated hydrogen peroxide was evaluated with an industrial wastewater. The copper (II) ions addition into the wastewater using electro-dissolution of copper electrodes, reduces the chemical oxygen demand (COD) by 56% after 30 min of treatment, under optimal conditions of pH 2,8 and 14.2 mA cm(-2) of current density. The integrated electrochemical process reduces the COD by 78%, BOD? by 81%, color by 97% and fecal coliforms by 99.9%. The wastewater quality was monitored using UV-Vis spectrometry and Z-potential in order to characterize raw and treated wastewater. PMID:24556544

  1. Bibliography on contaminants and solubility of organic compounds in oxygen

    NASA Technical Reports Server (NTRS)

    Ordin, P. M. (compiler)

    1975-01-01

    A compilation of a number of document citations is presented which contains information on contaminants in oxygen. Topics covered include contaminants and solubility of organic compounds in oxygen, reaction characteristics of organic compounds with oxygen, and sampling and detection limits of impurities. Each citation in the data bank contains many items of information about the document. Some of the items are title, author, abstract, corporate source, description of figures pertinent to hazards or safety, key references, and descriptors (keywords) by which the document can be retrieved. Each citation includes an evaluation of the technical contents as to being good/excellent, acceptable, or poor. The descriptors used to define the contents of the documents and subsequently used in the computerized search operations were developed for the cryogenic fluid safety by experts in the cryogenics field.

  2. Nonlinear Laser Fluorescence Spectroscopy of Natural Organic Compounds

    NASA Astrophysics Data System (ADS)

    Fadeev, Victor V.; Shirshin, Evgeny A.

    Principles of nonlinear laser fluorescence spectroscopy of complicated organic compounds and of the method capable of determining photophysical parameters are considered in this chapter. Special attention is paid to the peculiarities of the method connected with specific photophysical processes in natural organic compounds, especially in proteins, and to the major role of intramolecular energy transfer and presence of localized donor-acceptor pairs (LDAP) of fluorophores within single macromolecules. These facts stimulated the development of models based on the collective states formalism describing fluorescent response of LDAP to pulsed laser excitation. Unique features of the method are illustrated by the example of proteins (proteins with intrinsic fluorescence (HSA, BSA) and fluorescent protein mRFP1) that can be used as fluorescent tags of intracellular processes while their photophysical parameters can be used as the information channel.

  3. Emission of volatile organic compounds (VOCs) from PVC floor coverings.

    PubMed

    Wiglusz, R; Igielska, B; Sitko, E; Nikel, G; Jarnuszkiewicz, I

    1998-01-01

    In this study 29 PVC floor coverings were tested for emission of vinyl chloride (VC) and other volatile organic compounds (VOCs). A study on the effect of higher temperature on emission of VOCs from newly manufactured PVC flooring was also carried out. The study was conducted in climatic chamber, according to Polish Standard PN-89/Z-04021. GC method was used for analyzing of the compounds emitted. VC was not emitted from any of the floorings tested. Other VOCs were emitted in different concentrations. The influence of temperature on emission was conducted at temperatures of 23 degrees C and 35 degrees C from 2 hrs up to 180 days after introduction of materials in the chamber. The increase of temperature caused increase of total volatile organic compounds (TVOC) emission during 24 hrs of experiment. Then the emission was comparable for both temperatures. After 9 days emission of identified and unidentified compounds (TVOC) showed a rapid decay and stayed on very low level during a few months. The study conducted showed that PVC floorings after 10 days of installation in the room should not be source of indoor air contamination. PMID:10431652

  4. Pharmaceuticals, hormones, and other organic wastewater contaminants in U.S. streams, 1999-2000: A national reconnaissance

    USGS Publications Warehouse

    Kolpin, D.W.; Furlong, E.T.; Meyer, M.T.; Thurman, E.M.; Zaugg, S.D.; Barber, L.B.; Buxton, H.T.

    2002-01-01

    To provide the first nationwide reconnaissance of the occurrence of pharmaceuticals, hormones, and other organic wastewater contaminants (OWCs) in water resources, the U.S. Geological Survey used five newly developed analytical methods to measure concentrations of 95 OWCs in water samples from a network of 139 streams across 30 states during 1999 and 2000. The selection of sampling sites was biased toward streams susceptible to contamination (i.e. downstream of intense urbanization and livestock production). OWCs were prevalent during this study, being found in 80% of the streams sampled. The compounds detected represent a wide range of residential, industrial, and agricultural origins and uses with 82 of the 95 OWCs being found during this study. The most frequently detected compounds were coprostanol (fecal steroid), cholesterol (plant and animal steroid), N,N-diethyltoluamide (insect repellant), caffeine (stimulant), triclosan (antimicrobial disinfectant), tri(2-chloroethyl)phosphate (fire retardant), and 4-nonylphenol (nonionic detergent metabolite). Measured concentrations for this study were generally low and rarely exceeded drinking-water guidelines, drinking-water health advisories, or aquatic-life criteria. Many compounds, however, do not have such guidelines established. The detection of multiple OWCs was common for this study, with a median of seven and as many as 38 OWCs being found in a given water sample. Little is known about the potential interactive effects (such as synergistic or antagonistic toxicity) that may occur from complex mixtures of OWCs in the environment. In addition, results of this study demonstrate the importance of obtaining data on metabolites to fully understand not only the fate and transport of OWCs in the hydrologic system but also their ultimate overall effect on human health and the environment.

  5. Continuous electricity generation from domestic wastewater and organic substrates in a flat plate microbial fuel cell.

    PubMed

    Min, Booki; Logan, Bruce E

    2004-11-01

    A microbial fuel cell (MFC) is a device that converts organic matter to electricity using microorganisms as the biocatalyst. Most MFCs contain two electrodes separated into one or two chambers that are operated as a completely mixed reactor. In this study, a flat plate MFC (FPMFC) was designed to operate as a plug flow reactor (no mixing) using a combined electrode/proton exchange membrane (PEM) system. The reactor consisted of a single channel formed between two nonconductive plates that were separated into two halves by the electrode/PEM assembly. Each electrode was placed on an opposite side of the PEM, with the anode facing the chamber containing the liquid phase and the cathode facing a chamber containing only air. Electricity generation using the FPMFC was examined by continuously feeding a solution containing wastewater, or a specific substrate, into the anode chamber. The system was initially acclimated for 1 month using domestic wastewater orwastewater enriched with a specific substrate such as acetate. Average power density using only domestic wastewater was 72+/-1 mW/m2 at a liquid flow rate of 0.39 mL/min [42% COD (chemical oxygen demand) removal, 1.1 h HRT (hydraulic retention time)]. At a longer HRT = 4.0 h, there was 79% COD removal and an average power density of 43+/-1 mW/m2. Power output was found to be a function of wastewater strength according to a Monod-type relationship, with a half-saturation constant of Ks = 461 or 719 mg COD/L. Power generation was sustained at high rates with several organic substrates (all at approximately 1000 mg COD/L), including glucose (212+/-2 mW/ m2), acetate (286+/-3 mW/m2), butyrate (220+/-1 mW/ m2), dextran (150+/-1 mW/m2), and starch (242+/-3 mW/ m2). These results demonstrate the versatility of power generation in a MFC with a variety of organic substrates and show that power can be generated at a high rate in a continuous flow reactor system. PMID:15575304

  6. Sugar-Related Organic Compounds in Carbonaceous Meteorites

    NASA Technical Reports Server (NTRS)

    Cooper, G.; Kimmich, N.; Belisle, W.; Sarinana, J.; Brabham, K.; Garrel, L.; DeVincenzi, Donald L. (Technical Monitor)

    2001-01-01

    Sugars and related polyols are critical components of all organisms and may have been necessary for the origin of life. To date, this class of organic compounds had not been definitively identified in meteorites. This study was undertaken to determine if polyols were present in the early Solar System as constituents of carbonaceous meteorites. Results of analyses of the Murchison and Murray meteorites indicate that formaldehyde and sugar chemistry may be responsible for the presence of a variety of polyols. We conclude that polyols were present on the early Earth through delivery by asteroids and possibly comets.

  7. 40 CFR Table 37 to Subpart G of... - Default Biorates for List 1 Compounds

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...Pollutants From the Synthetic Organic Chemical Manufacturing Industry for Process Vents, Storage Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 37 Table 37 to Subpart G of Part 63—Default Biorates for List 1 Compounds Compound...

  8. 40 CFR Table 37 to Subpart G of... - Default Biorates for List 1 Compounds

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...Pollutants From the Synthetic Organic Chemical Manufacturing Industry for Process Vents, Storage Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 37 Table 37 to Subpart G of Part 63—Default Biorates for List 1 Compounds Compound...

  9. HS-SPME/GC-MS analysis of volatile and semi-volatile organic compounds emitted from municipal sewage sludge.

    PubMed

    Kotowska, Urszula; ?alikowski, Maciej; Isidorov, Valery A

    2012-05-01

    The aim of the research involved identification and semi-quantitative determination of unknown volatile and semi-volatile organic compounds emitted to air by sewage sludge formed in the process of municipal wastewater treatment in a sewage treatment plant. Samples taken directly after completion of the technological process as well as the sludge stored on the premise of the sewage treatment plant were analyzed. A simple method using off-line headspace solid-phase microextraction combined with gas chromatography-mass spectrometry has been proposed for extraction and detection of organic pollutants. For reliable identification of compounds, combination of two independent parameters: mass spectra and linear temperature programmed retention indices were employed. Over 170 compounds of different structure were identified including aliphatic and aromatic hydrocarbons, alcohols, esters, carbonyls, as well as sulfur, nitrogen, and chlorine containing compounds. The prevailing substances included: ethyl ether, n-hexane, p-xylene, o-xylene, mesitylene, m-ethylbenzene, limonene, n-decane, n-undecane, and n-dodecane. A few compounds such as methanetiol, dimethyl polisulfide, octaatomic sulfur, phthalic anhydride, and indoles were identified in the sludge for the first time. PMID:21688031

  10. Removal and fate of trace organic compounds in microbial fuel cells.

    PubMed

    Wang, Heming; Heil, Dean; Ren, Zhiyong Jason; Xu, Pei

    2015-04-01

    This study focused on understanding and characterizing the removal of trace organic compounds (TOrCs) in microbial fuel cells (MFC). 26 TOrCs with broad physicochemical properties were spiked in synthetic wastewater. Single-chamber air-cathode MFC (SMFC) and double-chamber air-cathode MFC (DMFC) were constructed to provide combined or separated oxidation/reduction environments for TOrCs removal. The study showed that TOrCs removal processes involved both sorption and biodegradation. For neutral TOrCs, the removal efficiency was affected primarily by the biodegradability probability and hydrophobicity of the compounds, while electrostatic interactions played an additional role in the MFCs as the removal of positively charged TOrCs was generally higher than negatively charged TOrCs. The presence of TOrCs showed negligible impact on MFC power generation, likewise the operation of MFCs had marginal effect on TOrCs removal, except longer residence time in MFCs improved biological removal performance. PMID:25532765

  11. Effects of effluent organic matter characteristics on the removal of bulk organic matter and selected pharmaceutically active compounds during managed aquifer recharge: Column study.

    PubMed

    Maeng, Sung Kyu; Sharma, Saroj K; Abel, Chol D T; Magic-Knezev, Aleksandra; Song, Kyung-Guen; Amy, Gary L

    2012-10-01

    Soil column experiments were conducted to investigate the effects of effluent organic matter (EfOM) characteristics on the removal of bulk organic matter (OM) and pharmaceutically active compounds (PhACs) during managed aquifer recharge (MAR) treatment processes. The fate of bulk OM and PhACs during an MAR is important to assess post-treatment requirements. Biodegradable OM from EfOM, originating from biological wastewater treatment, was effectively removed during soil passage. Based on a fluorescence excitation-emission matrix (F-EEM) analysis of wastewater effluent-dominated (WWE-dom) surface water (SW), protein-like substances, i.e., biopolymers, were removed more favorably than fluorescent humic-like substances under oxic compared to anoxic conditions. However, there was no preferential removal of biopolymers or humic substances, determined as dissolved organic carbon (DOC) observed via liquid chromatography with online organic carbon detection (LC-OCD) analysis. Most of the selected PhACs exhibited removal efficiencies of greater than 90% in both SW and WWE-dom SW. However, the removal efficiencies of bezafibrate, diclofenac and gemfibrozil were relatively low in WWE-dom SW, which contained more biodegradable OM than did SW (copiotrophic metabolism). Based on this study, low biodegradable fractions such as humic substances in MR may have enhanced the degradation of diclofenac, gemfibrozil and bezafibrate by inducing an oligotrophic microbial community via long term starvation. Both carbamazepine and clofibric acid showed persistent behaviors and were not influenced by EfOM. PMID:23026644

  12. Effects of effluent organic matter characteristics on the removal of bulk organic matter and selected pharmaceutically active compounds during managed aquifer recharge: Column study

    NASA Astrophysics Data System (ADS)

    Maeng, Sung Kyu; Sharma, Saroj K.; Abel, Chol D. T.; Magic-Knezev, Aleksandra; Song, Kyung-Guen; Amy, Gary L.

    2012-10-01

    Soil column experiments were conducted to investigate the effects of effluent organic matter (EfOM) characteristics on the removal of bulk organic matter (OM) and pharmaceutically active compounds (PhACs) during managed aquifer recharge (MAR) treatment processes. The fate of bulk OM and PhACs during an MAR is important to assess post-treatment requirements. Biodegradable OM from EfOM, originating from biological wastewater treatment, was effectively removed during soil passage. Based on a fluorescence excitation-emission matrix (F-EEM) analysis of wastewater effluent-dominated (WWE-dom) surface water (SW), protein-like substances, i.e., biopolymers, were removed more favorably than fluorescent humic-like substances under oxic compared to anoxic conditions. However, there was no preferential removal of biopolymers or humic substances, determined as dissolved organic carbon (DOC) observed via liquid chromatography with online organic carbon detection (LC-OCD) analysis. Most of the selected PhACs exhibited removal efficiencies of greater than 90% in both SW and WWE-dom SW. However, the removal efficiencies of bezafibrate, diclofenac and gemfibrozil were relatively low in WWE-dom SW, which contained more biodegradable OM than did SW (copiotrophic metabolism). Based on this study, low biodegradable fractions such as humic substances in MR may have enhanced the degradation of diclofenac, gemfibrozil and bezafibrate by inducing an oligotrophic microbial community via long term starvation. Both carbamazepine and clofibric acid showed persistent behaviors and were not influenced by EfOM.

  13. Unit Process Wetlands for Removal of Trace Organic Contaminants and Pathogens from Municipal Wastewater Effluents

    PubMed Central

    Jasper, Justin T.; Nguyen, Mi T.; Jones, Zackary L.; Ismail, Niveen S.; Sedlak, David L.; Sharp, Jonathan O.; Luthy, Richard G.; Horne, Alex J.; Nelson, Kara L.

    2013-01-01

    Abstract Treatment wetlands have become an attractive option for the removal of nutrients from municipal wastewater effluents due to their low energy requirements and operational costs, as well as the ancillary benefits they provide, including creating aesthetically appealing spaces and wildlife habitats. Treatment wetlands also hold promise as a means of removing other wastewater-derived contaminants, such as trace organic contaminants and pathogens. However, concerns about variations in treatment efficacy of these pollutants, coupled with an incomplete mechanistic understanding of their removal in wetlands, hinder the widespread adoption of constructed wetlands for these two classes of contaminants. A better understanding is needed so that wetlands as a unit process can be designed for their removal, with individual wetland cells optimized for the removal of specific contaminants, and connected in series or integrated with other engineered or natural treatment processes. In this article, removal mechanisms of trace organic contaminants and pathogens are reviewed, including sorption and sedimentation, biotransformation and predation, photolysis and photoinactivation, and remaining knowledge gaps are identified. In addition, suggestions are provided for how these treatment mechanisms can be enhanced in commonly employed unit process wetland cells or how they might be harnessed in novel unit process cells. It is hoped that application of the unit process concept to a wider range of contaminants will lead to more widespread application of wetland treatment trains as components of urban water infrastructure in the United States and around the globe. PMID:23983451

  14. Reuse of spent granular activated carbon for organic micro-pollutant removal from treated wastewater.

    PubMed

    Hu, Jingyi; Shang, Ran; Heijman, Bas; Rietveld, Luuk

    2015-09-01

    Spent granular activated carbons (sGACs) for drinking water treatments were reused via pulverizing as low-cost adsorbents for micro-pollutant adsorption from a secondary treated wastewater effluent. The changes of physicochemical characteristics of the spent carbons in relation to the fresh carbons were determined and were correlated to the molecular properties of the respective GAC influents (i.e. a surface water and a groundwater). Pore size distribution analysis showed that the carbon pore volume decreased over a wider size range due to preloading by surface water, which contains a broader molecular weight distribution of organic matter in contrast to the groundwater. However, there was still considerable capacity available on the pulverized sGACs for atrazine adsorption in demineralized water and secondary effluent, and this was particularly the case for the groundwater spent GAC. However, as compared to the fresh counterparts, the decreased surface area and the induced surface acidic groups on the pulverized sGACs contributed both to the lower uptake and the more impeded adsorption kinetic of atrazine in the demineralized water. Nonetheless, the pulverized sGACs, especially the one preloaded by surface water, was less susceptible to adsorption competition in the secondary effluent, due to its negatively charged surface which can repulse the accessibility of the co-present organic matter. This suggests the reusability of the drinking water spent GACs for micro-pollutant adsorption in the treated wastewater. PMID:26093103

  15. Simultaneous removal of organic matter and nitrogen compounds by combining a membrane bioreactor and a membrane biofilm reactor.

    PubMed

    Hasar, Halil

    2009-05-01

    Hydrogen-based membrane biofilm reactors (MBfR) have been applied to the denitrification of nitrate-containing water and wastewater. Adding an aerobic membrane bioreactor (MBR) to a MBfR provides significant nitrification and organic oxidation because most wastewater also contains a significant concentration of organic material and ammonium nitrogen. This study describes experiments that investigate the removal of organic and nitrogenous compounds in the combined MBR/MBfR system. The experiments demonstrate that the MBR/MBfR combination successfully performs COD oxidation and nitrogen removal for organic and ammonium loads in the ranges of 1000-4300gCOD/m(3)-d and 200-230gN/m(3)-d, respectively. Total-nitrogen removal was controlled by nitrification in the MBR, because the MBfR denitrified all of the NO(3)(-) provided by the MBR. The nitrate flux in the MBfR was in the range of 4-8gN/m(2)-d for cases of almost complete denitrification (>99 %); the H(2) flux was varied from 1.4 to 2.8gH(2)/m(2)-d. PMID:19186053

  16. PARTITION EQUILIBRIA OF NONIONIC ORGANIC COMPOUNDS BETWEEN SOIL ORGANIC MATTER AND WATER

    EPA Science Inventory

    Equilibrium isotherms for the simultaneous uptake of binary nonionic organic compounds from water on soil indicated no competitive effect between the two solutes. The observation supports the hypothesis that partition to the soil organic phase is the primary process for sorption ...

  17. Measurements of halogenated organic compounds near the tropical tropopause

    SciTech Connect

    Schauffler, S.M.; Heidt, L.E.; Pollock, W.H.; Gilpin, T.M.; Lueb, R.A.; Atlas, E.L. ); Vedder, J.F. ); Solomon, S. )

    1993-11-19

    The amount of organic chlorine and bromine entering the stratosphere have a direct influence on the magnitude of chlorine and bromine catalyzed ozone losses. Twelve organic chlorine species and five organic bromine species were measured from 12 samples collected near the tropopause between 23.8[degrees]N and 25.3[degrees]N during AASE II. The average mixing ratios of total organic chlorine and total organic bromine were 3.50 [+-] 0.06 ppbv and 21.1 [+-] 0.8 pptv, respectively. CH[sub 3]Cl represented 15.1% of the total organic chlorine, with CFC 11 (CCl[sub 3]F) and CFC 12 (CCl[sub 2]F[sub 2]) accounting for 22.6% and 28.2%, respectively, with the remaining 34.1% primarily from CCl[sub 4], CH[sub 3]CCl[sub 3], and CFC 113 (CCl[sub 2]FCClF[sub 2]). CH[sub 3]Br represented 54% of the total organic bromine. The 95% confidence intervals of the mixing ratios of all but four of the individual compounds were within the range observed in low and mid-latitude mid-troposphere samples. The four compounds with significantly lower mixing ratios at the tropopause were CHCl[sub 3], CH[sub 2]Cl[sub 2], CH[sub 2]Br[sub 2], and CH[sub 3]CCl[sub 3]. The lower mixing ratios may be due to entrainment of southern hemisphere air during vertical transport in the tropical region and/or to exchange of air across the tropopause between the lower stratosphere and upper troposphere. 14 refs., 3 tabs.

  18. 40 CFR Table 9 to Subpart G of... - Organic HAP's Subject to the Wastewater Provisions for Process Units at New and Existing Sources...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 9 2011-07-01 2011-07-01 false Organic HAP's Subject to the Wastewater... Chemical Manufacturing Industry for Process Vents, Storage Vessels, Transfer Operations, and Wastewater Pt. 63, Subpt. G, Table 9 Table 9 to Subpart G of Part 63—Organic HAP's Subject to the...

  19. Simulation of Comet Impact and Survivability of Organic Compounds

    SciTech Connect

    Liu, B T; Lomov, I N; Blank, J G; Antoun, T H

    2007-07-18

    Comets have long been proposed as a potential means for the transport of complex organic compounds to early Earth. For this to be a viable mechanism, a significant fraction of organic compounds must survive the high temperatures due to impact. We have undertaken three-dimensional numerical simulations to track the thermodynamic state of a comet during oblique impacts. The comet was modeled as a 1-km water-ice sphere impacting a basalt plane at 11.2 km/s; impact angles of 15{sup o} (from horizontal), 30{sup o}, 45{sup o}, 65{sup o}, and 90{sup o} (normal impact) were examined. The survival of organic cometary material, modeled as water ice for simplicity, was calculated using three criteria: (1) peak temperatures, (2) the thermodynamic phase of H{sub 2}O, and (3) final temperature upon isentropic unloading. For impact angles greater than or equal to 30{sup o}, no organic material is expected to survive the impact. For the 15{sup o} impact, most of the material survives the initial impact and significant fractions (55%, 25%, and 44%, respectively) satisfy each survival criterion at 1 second. Heating due to deceleration, in addition to shock heating, plays a role in the heating of the cometary material for nonnormal impacts. This effect is more noticeable for more oblique impacts, resulting in significant deviations from estimates using scaling of normal impacts. The deceleration heating of the material at late times requires further modeling of breakup and mixing.

  20. Contribution of organosulfur compounds to organic aerosol mass.

    PubMed

    Tolocka, Michael P; Turpin, Barbara

    2012-08-01

    Organosulfates have been proposed as products of secondary organic aerosol formation. While organosulfates have been identified in ambient aerosol samples, a question remains as to the magnitude of their contribution to particulate organic mass. At the same time, discrepancies have been observed between total particulate sulfur measured by X-ray fluorescence (XRF) spectroscopy and sulfur present as inorganic sulfate measured by ion chromatography (IC) in fine particulate matter. These differences could be attributed to measurement bias and/or the contribution of other sulfur compounds, including organosulfates. Using the National Park Service IMPROVE PM(2.5) database, we examined the disparity between the sulfur and sulfate measurements at 12 sites across the United States to provide upper-bound estimates for the annual average contributions of organosulfates to organic mass. The data set consists of over 150000 measurements. The 12 sites include Brigantine, NJ, Cape Cod, MA, Washington, DC, Chassahowitzka, FL, Great Smoky Mountains National Park, NC, Okefenokee, GA, Bondville, IL, Mingo, MO, Phoenix, AZ, San Gabriel, CA, Crater Lake National Park, OR, and Spokane, WA. These sites are representative of the different regions of the country: Northeast, Southeast, Midwest, Southwest and Northwest. We estimate that organosulfur compounds could comprise as much as 5-10% of the organic mass at these sites. The contribution varies by season and location and appears to be higher during warm months when photochemical oxidation chemistry is most active. PMID:22731120

  1. Characteristics of the volatile organic compounds -- Arid Integrated Demonstration Site

    SciTech Connect

    Last, G.V.; Lenhard, R.J.; Bjornstad, B.N.; Evans, J.C.; Roberson, K.R.; Spane, F.A.; Amonette, J.E.; Rockhold, M.L.

    1991-10-01

    The Volatile Organic Compounds -- Arid Integrated Demonstration Program (VOC-Arid ID) is targeted at demonstration and testing of technologies for the evaluation and cleanup of volatile organic compounds and associated contaminants at arid DOE sites. The initial demonstration site is an area of carbon tetrachloride (CCl{sub 4}) contamination located near the center of the Hanford Site. The movement of CCl{sub 4} and other volatile organic contaminants in the subsurface is very complex. The problem at the Hanford Site is further complicated by the concurrent discharge of other waste constituents including acids, lard oil, organic phosphates, and transuranic radionuclides. In addition, the subsurface environment is very complex, with large spatial variabilities in hydraulic properties. A thorough understanding of the problem is essential to the selection of appropriate containment, retrieval, and/or in situ remedial technologies. The effectiveness of remedial technologies depends on knowing where the contaminants are, how they are held up in a given physical and chemical subsurface environment; and knowing the physical, chemical, and microbiological changes that are induced by the various remedial technologies.

  2. Commuter exposure to volatile organic compounds under different driving conditions

    NASA Astrophysics Data System (ADS)

    Jo, Wan-Kuen; Park, Kun-Ho

    The driving conditions that were tested for the in-vehicle concentrations of selected volatile organic compounds (VOCs) included transport modes, fuel distributions, vehicle ventilation conditions, driving routes, commute seasons, car models, and driving periods. This study involved two sampling seasons (winter and summer). The in-auto/in-bus/fixed site ratio of the wintertime mean concentrations was about 6/3/1 for total VOCs and 8/3/1 for benzene. On the median, the in-auto/in-bus exposure ratio ranged from 1.5 to 2.8 for the morning commutes, and ranged from 2.4 to 4.5 for evening commutes, depending on the target compounds. The wintertime in-auto concentrations were significantly higher ( p<0.05), on the average 3-5 times higher, in a carbureted engine than in the three electronic fuel-injected cars. For the summertime in-auto concentrations of the target compounds except benzene, there were no significant differences between low and high ventilation conditions on the two urban routes. The urban in-auto benzene concentration was significantly higher ( p<0.05) under the low ventilation condition. For the rural commutes, the in-auto concentrations of all target compounds were significantly higher ( p<0.05) under the low ventilation condition. The in-auto VOC concentrations on the two urban routes did not differ significantly, and they were greater than the rural in-auto concentrations, with the differences being significant ( p<0.05) for all target compounds. The summertime in-auto concentrations of benzene and toluene were greater than the wintertime in-auto concentrations, with the difference being significant ( p<0.05), while the concentrations of the other target compounds were not significantly different between the two seasons. Neither car models nor driving periods influenced the in-auto VOC concentrations.

  3. Selective Sorption of Dissolved Organic Carbon Compounds by Temperate Soils

    SciTech Connect

    Jagadamma, Sindhu; Mayes, Melanie; Phillips, Jana Randolph

    2012-01-01

    Physico-chemical sorption of dissolved organic carbon (DOC) on soil minerals is one of the major processes of organic carbon (OC) stabilization in soils, especially in deeper layers. The attachment of C on soil solids is related to the reactivity of the soil minerals and the chemistry of the sorbate functional groups, but the sorption studies conducted without controlling microbial activity may overestimate the sorption potential of soil. This study was conducted to examine the sorptive characteristics of a diverse functional groups of simple OC compounds (D-glucose, L-alanine, oxalic acid, salicylic acid, and sinapyl alcohol) on temperate climate soil orders (Mollisols, Ultisols and Alfisols) with and without biological degradative processes. Equilibrium batch experiments were conducted using 0-100 mg C L-1 at a solid-solution ratio of 1:60 for 48 hrs and the sorption parameters were calculated by Langmuir model fitting. The amount of added compounds that remained in the solution phase was detected by high performance liquid chromatography (HPLC) and total organic C (TOC) analysis. Soil sterilization was performed by -irradiation technique and experiments were repeated to determine the contribution of microbial degradation to apparent sorption. Overall, Ultisols did not show a marked preference for apparent sorption of any of the model compounds, as indicated by a narrower range of maximum sorption capacity (Smax) of 173-527 mg kg soil-1 across compounds. Mollisols exhibited a strong preference for apparent sorption of oxalic acid (Smax of 5290 mg kg soil-1) and sinapyl alcohol (Smax of 2031 mg kg soil-1) over the other compounds. The propensity for sorption of oxalic acid is mainly attributed to the precipitation of insoluble Ca-oxalate due to the calcareous nature of most Mollisol subsoils and its preference for sinapyl alcohol could be linked to the polymerization of this lignin monomer on 2:2 mineral dominated soils. The reactivity of Alfisols to DOC was in between that of Ultisols and Mollisols. HPLC results revealed significantly higher sorption of D-glucose and L-alanine than did TOC results, and duplicate experiments with sterilized soils confirmed that glucose and alanine were mineralized leading to higher apparent sorption values via HPLC. This study demonstrated that three common temperate soil orders experienced differential sorption of simple OC compounds, indicating that sorbate chemistry plays a significant role in the sorptive stabilization of DOC.

  4. Evaluation of 4-nitrophenol ELISA kit for assessing the origin of organic pollution in wastewater treatment works

    SciTech Connect

    La Farre, M.; Oubina, A.; Marco, M.P.; Ginebreda, A.; Tirapu, L.; Barcelo, D.

    1999-11-01

    A cost-effective strategy based on a recently developed ELISA for 4-nitrophenol was used for the characterization of wastewater samples (industrial and/or urban) of the primary sewage effluent and secondary sewage effluent, also called influent and effluent, respectively, of wastewater treatment works (WWTW) using either biological treatment with secondary settlement and/or physicochemical treatment. Two of the WWTW received only domestic wastewaters, whereas three of them received 60--70% of industrial effluents that were mixed with domestic wastewaters before entering WWTW. The 4-nitrophenol ELISA kit was used as a parameter to evaluate the performance of the treatment plants by comparing the ELISA measurements with those routinely used in WWTW, such as total organic carbon and total phenols content using 4-aminoantipyrine. The 4-nitrophenol ELISA gave a positive response to different wastewaters being a useful measurement for the estimation of the performance of the WWTW. The response obtained with 4-nitrophenol ELISA can differentiate the wastewater pollution discharged into WWTW, either from domestic or industrial sources.

  5. Dissolved organic compounds in reused process water for steam-assisted gravity drainage oil sands extraction.

    PubMed

    Kawaguchi, Hideo; Li, Zhengguo; Masuda, Yoshihiro; Sato, Kozo; Nakagawa, Hiroyuki

    2012-11-01

    The in situ oil sands production method called steam-assisted gravity drainage (SAGD) reuses process wastewater following treatment. However, the treatment and reuse processes concentrate contaminants in the process water. To determine the concentration and dynamics of inorganic and organic contaminants, makeup water and process water from six process steps were sampled at a facility employing the SAGD process in Alberta, Canada. In the groundwater used for the makeup water, the total dissolved organic carbon (DOC) content was 4 mg/L. This significantly increased to 508 mg/L in the produced water, followed by a gradual increase with successive steps in subsequent water treatments. The concentrations and dynamics of DOC constituents in the process water determined by gas chromatography-mass spectrometry showed that in the produced water, volatile organic compounds (VOCs) such as acetone (33.1 mg/L) and 2-butanone (13.4 mg/L) predominated, and there were significant amounts of phenolic compounds (total 9.8 mg/L) and organic acids including naphthenic acids (NAs) corresponding to the formula C(n)H(2n+Z)O(X) for combinations of n = 4 to 18, Z = 0 and -2, and X = 2 to 4 (53 mg/L) with trace amounts of polycyclic aromatic hydrocarbons (PAHs) such as naphthalene and phenanthrene. No organic contaminants, except for saturated fatty acids, were detected in the groundwater. The concentration of DOC in the recycled water was 4.4-fold higher than that in the produced water. Likewise, the total concentrations of phenols and organic acids in the recycled water were 1.7- and 4.5-fold higher than in the produced water, whereas the total concentrations of VOCs and PAHs in the recycled water were reduced by over 80%, suggesting that phenols and organic acids are selectively concentrated in the process water treatment. This comprehensive chemical analysis thus identified organic constituents that were concentrated in the process water and which interfere with subsequent water treatments in the SAGD process. PMID:22901407

  6. Global simulation of aromatic volatile organic compounds in the atmosphere

    NASA Astrophysics Data System (ADS)

    Cabrera Perez, David; Taraborrelli, Domenico; Pozzer, Andrea

    2015-04-01

    Among the large number of chemical compounds in the atmosphere, the organic group plays a key role in the tropospheric chemistry. Specifically the subgroup called aromatics is of great interest. Aromatics are the predominant trace gases in urban areas due to high emissions, primarily by vehicle exhausts and fuel evaporation. They are also present in areas where biofuel is used (i.e residential wood burning). Emissions of aromatic compounds are a substantial fraction of the total emissions of the volatile organic compounds (VOC). Impact of aromatics on human health is very important, as they do not only contribute to the ozone formation in the urban environment, but they are also highly toxic themselves, especially in the case of benzene which is able to trigger a range of illness under long exposure, and of nitro-phenols which cause detrimental for humans and vegetation even at very low concentrations. The aim of this work is to assess the atmospheric impacts of aromatic compounds on the global scale. The main goals are: lifetime and budget estimation, mixing ratios distribution, net effect on ozone production and OH loss for the most emitted aromatic compounds (benzene, toluene, xylenes, ethylbenzene, styrene and trimethylbenzenes). For this purpose, we use the numerical chemistry and climate simulation ECHAM/MESSy Atmospheric Chemistry (EMAC) model to build the global atmospheric budget for the most emitted and predominant aromatic compounds in the atmosphere. A set of emissions was prepared in order to include biomass burning, vegetation and anthropogenic sources of aromatics into the model. A chemical mechanism based on the Master Chemical Mechanism (MCM) was developed to describe the chemical oxidation in the gas phase of these aromatic compounds. MCM have been reduced in terms of number of chemical equation and species in order to make it affordable in a 3D model. Additionally other features have been added, for instance the production of HONO via ortho-nitrophenols photolysis. The model results are compared with observations from different surface and aircraft campaigns in order to estimate the accuracy of the model.

  7. Multiple microbial activities for volatile organic compounds reduction by biofiltration.

    PubMed

    Civilini, Marcello

    2006-07-01

    In the northeast of Italy, high volatile organic carbon (VOC) emissions originate from small-medium companies producing furniture. In these conditions it is difficult to propose a single, efficient, and economic system to reduce pollution. Among the various choices, the biofiltration method could be a good solution, because microbial populations possess multiple VOC degradation potentials used to oxidize these compounds to CO2. Starting from the air emissions of a typical industrial wood-painting plant, a series of experiments studied in vitro microbial degradation of each individual VOC. Isolated strains were then added to a laboratory-scale biofiltration apparatus filled with an organic matrix, and the different VOC behavior demonstrated the potential of single and/or synergic microbial removal actions. When a single substrate was fed, the removal efficiency of a Pseudomonas aeruginosa inoculated reactor was 1.1, 1.17, and 0.33 g m(-3) hr(-1), respectively, for xylene, toluene, and ethoxy propyl acetate. A VOC mixture composed of butyl acetate, ethyl acetate, diacetin alcohol, ethoxy propanol acetate, methyl ethyl ketone, methyl isobutyl ketone, toluene, and xylene was then fed into a 2-m(3) reactor treating 100 m3 hr(-1) of contaminated air. The reactor was filled with the same mixture of organic matrix, enriched with all of the isolated strains together. During reactor study, different VOC loading rates were used, and the behavior was evaluated continuously. After a short acclimation period, the removal efficiency was > 65% at VOC load of 150-200 g m(-3) hr(-1). Quantification of removal efficiencies and VOC speciation confirmed the relationship among removal efficiencies, compound biodegradability, and the dynamic transport of each mixture component within the organic matrix. Samples of the fixed bed were withdrawn at different intervals and the heterogeneous microbial community evaluated for both total and differential compound counts. PMID:16878585

  8. Transport, behavior, and fate of volatile organic compounds in streams

    USGS Publications Warehouse

    Rathbun, R.E.

    2000-01-01

    Volatile organic compounds (VOCs) are compounds with chemical and physical properties that allow the compounds to move freely between the water and air phases of the environment. VOCs are widespread in the environment because of this mobility. Many VOCs have properties that make them suspected or known hazards to the health of humans and aquatic organisms. Consequently, understanding the processes affecting the concentration and distribution of VOCs in the environment is necessary. The transport, behavior, and fate of VOCs in streams are determined by combinations of chemical, physical, and biological processes. These processes are volatilization, absorption, wet and dry deposition, microbial degradation, sorption, hydrolysis, aquatic photolysis, oxidation, chemical reaction, biocon-centration, advection, and dispersion. The relative importance of each of these processes depends on the characteristics of the VOC and the stream. The U.S. Geological Survey National Water-Quality Assessment Program selected 55 VOCs for study. This article reviews the characteristics of the various processes that could affect the transport, behavior, and fate of these VOCs in streams.

  9. Measurement of volatile organic compounds in human blood.

    PubMed Central

    Ashley, D L; Bonin, M A; Cardinali, F L; McCraw, J M; Wooten, J V

    1996-01-01

    Volatile organic compounds (VOCs) are an important public health problem throughout the developed world. Many important questions remain to be addressed in assessing exposure to these compounds. Because they are ubiquitous and highly volatile, special techniques must be applied in the analytical determination of VOCs. The analytical methodology chosen to measure toxicants in biological materials must be well validated and carefully carried out; poor quality assurance can lead to invalid results that can have a direct bearing on treating exposed persons. The pharmacokinetics of VOCs show that most of the internal dose of these compounds is quickly eliminated, but there is a fraction that is only slowly removed, and these compounds may bioaccumulate. VOCs are found in the general population at the high parts-per-trillion range, but some people with much higher levels have apparently been exposed to VOC sources away from the workplace. Smoking is the most significant confounder to internal dose levels of VOCs and must be considered when evaluating suspected cases of exposure. PMID:8933028

  10. Lab-testing, predicting, and modeling multi-stage activated carbon adsorption of organic micro-pollutants from treated wastewater.

    PubMed

    Zietzschmann, F; Altmann, J; Hannemann, C; Jekel, M

    2015-10-15

    Multi-stage reuse of powdered activated carbon (PAC) is often applied in practice for a more efficient exploitation of the PAC capacity to remove organic micro-pollutants (OMP). However, the adsorption mechanisms in multi-stage PAC reuse are rarely investigated, as large-scale experiments do not allow for systematic tests. In this study, a laboratory method for the separation of PAC/water suspensions and the subsequent reuse of the PAC and the water was developed. The method was tested on wastewater treatment plant (WWTP) effluent in a setup with up to 7 PAC reuse stages. The tests show that the overall OMP removal from WWTP effluent can be increased when reusing PAC. The reason is that a repeated adsorption in multi-stage PAC reuse results in similar equilibrium concentrations as a single-stage adsorption. Thus, a single relationship between solid and liquid phase OMP concentrations appears valid throughout all stages. This also means that the adsorption efficiency of multi-stage PAC reuse setups can be estimated from the data of a single-stage setup. Furthermore, the overall OMP removals in multi-stage setups coincide with the overall UV254 removals, and for each respective OMP one relationship to UV254 removal is valid throughout all stages. The results were modeled by a simple modification of the equivalent background compound model (EBCM) which was also used to simulate the additional OMP removals in multi-stage setups with up to 50 reuse stages. PMID:26117373

  11. EVALUATION OF CRYOGENIC TRAPPING AS A MEANS FOR COLLECTING ORGANIC COMPOUNDS IN AMBIENT AIR

    EPA Science Inventory

    The methodology used in reduced temperature preconcentration of volatile organic compounds has been tested using a prototype automated gas chromatographic system. Mixtures of sixteen volatile organic compounds in humidified zero air were passed through a Nafion tube dryer and the...

  12. 40 CFR 60.542a - Alternate standard for volatile organic compounds.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 false Alternate standard for volatile organic compounds. 60.542a Section 60.542a Protection...Industry § 60.542a Alternate standard for volatile organic compounds. (a) On and after the date on...

  13. 40 CFR 60.502 - Standard for Volatile Organic Compound (VOC) emissions from bulk gasoline terminals.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...Organic Compound (VOC) emissions from bulk gasoline terminals. 60.502 Section 60...SOURCES Standards of Performance for Bulk Gasoline Terminals § 60.502 Standard for...Organic Compound (VOC) emissions from bulk gasoline terminals. On and after the...

  14. 40 CFR 60.502 - Standard for Volatile Organic Compound (VOC) emissions from bulk gasoline terminals.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...Organic Compound (VOC) emissions from bulk gasoline terminals. 60.502 Section 60...SOURCES Standards of Performance for Bulk Gasoline Terminals § 60.502 Standard for...Organic Compound (VOC) emissions from bulk gasoline terminals. On and after the...

  15. 40 CFR 60.502 - Standard for Volatile Organic Compound (VOC) emissions from bulk gasoline terminals.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...Organic Compound (VOC) emissions from bulk gasoline terminals. 60.502 Section 60...SOURCES Standards of Performance for Bulk Gasoline Terminals § 60.502 Standard for...Organic Compound (VOC) emissions from bulk gasoline terminals. On and after the...

  16. 40 CFR 60.502 - Standard for Volatile Organic Compound (VOC) emissions from bulk gasoline terminals.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...Organic Compound (VOC) emissions from bulk gasoline terminals. 60.502 Section 60...SOURCES Standards of Performance for Bulk Gasoline Terminals § 60.502 Standard for...Organic Compound (VOC) emissions from bulk gasoline terminals. On and after the...

  17. 40 CFR 60.502 - Standard for Volatile Organic Compound (VOC) emissions from bulk gasoline terminals.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...Organic Compound (VOC) emissions from bulk gasoline terminals. 60.502 Section 60...SOURCES Standards of Performance for Bulk Gasoline Terminals § 60.502 Standard for...Organic Compound (VOC) emissions from bulk gasoline terminals. On and after the...

  18. 40 CFR 60.112 - Standard for volatile organic compounds (VOC).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 false Standard for volatile organic compounds (VOC...Storage Vessels for Petroleum Liquids for Which Construction... § 60.112 Standard for volatile organic compounds (VOC...applies shall store petroleum liquids as follows: (1) If...

  19. 40 CFR 60.112a - Standard for volatile organic compounds (VOC).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 false Standard for volatile organic compounds (VOC...Storage Vessels for Petroleum Liquids for Which Construction... § 60.112a Standard for volatile organic compounds (VOC...which contains a petroleum liquid which, as stored,...

  20. Identification of some factors affecting pharmaceutical active compounds (PhACs) removal in real wastewater. Case study of fungal treatment of reverse osmosis concentrate.

    PubMed

    Badia-Fabregat, Marina; Lucas, Daniel; Gros, Meritxell; Rodríguez-Mozaz, Sara; Barceló, Damiŕ; Caminal, Glňria; Vicent, Teresa

    2015-02-11

    Many technologies are being developed for the efficient removal of micropollutants from wastewater and, among them, fungal degradation is one of the possible alternative biological treatments. In this article, some factors that might affect pharmaceutically active compounds (PhACs) removal in a fungal treatment of real wastewater were identified in batch bioreactor treating reverse osmosis concentrate (ROC) from urban wastewater treatment plant (WWTP). We found that degradation of PhACs by Trametes versicolor was enhanced by addition of external nutrients (global removal of 44%). Moreover, our results point out that high aeration might be involved in the increase in the concentration of some PhACs. In fact, conjugation and deconjugation processes (among others) affect the removal assessment of emerging contaminants when working with real concentrations in comparison to experiments with spiked samples. Moreover, factors that could affect the quantification of micropollutants at lab-scale experiments were studied. PMID:25464308

  1. Pharmaceutically active compounds in sludge stabilization treatments: anaerobic and aerobic digestion, wastewater stabilization ponds and composting.

    PubMed

    Martín, Julia; Santos, Juan Luis; Aparicio, Irene; Alonso, Esteban

    2015-01-15

    Sewage sludge disposal onto lands has been stabilized previously but still many pollutants are not efficiently removed. Special interest has been focused on pharmaceutical compounds due to their potential ecotoxicological effects. Nowadays, there is scarce information about their occurrence in different sludge stabilization treatments. In this work, the occurrence of twenty-two pharmaceutically active compounds has been studied in sludge from four sludge stabilization treatments: anaerobic digestion, aerobic digestion, composting and lagooning. The types of sludge evaluated were primary, secondary, anaerobically-digested and dehydrated, composted, mixed, aerobically-digested and dehydrated and lagoon sludge. Nineteen of the twenty-two pharmaceutically active compounds monitored were detected in sewage sludge. The most contaminated samples were primary sludge, secondary sludge and mixed sludge (the average concentrations of studied compounds in these sludges were 179, 310 and 142 ?g/kg dm, respectively) while the mean concentrations found in the other types of sewage sludge were 70 ?g/kg dm (aerobically-digested sludge), 63 ?g/kg dm (lagoon sludge), 12 ?g/kg dm (composted sludge) and 8 ?g/kg dm (anaerobically-digested sludge). The antibiotics ciprofloxacin and norfloxacin were found at the highest concentration levels in most of the analyzed sludge samples (up to 2660 and 4328 ?g/kg dm, respectively). Anaerobic-digestion treatment reduced more considerably the concentration of most of the studied compounds than aerobic-digestion (especially in the case of bezafibrate and fluoroquinolones) and more than anaerobic stabilization ponds (in the case of acetaminophen, atenolol, bezafibrate, carbamazepine, 17?-ethinylestradiol, naproxen and salicylic acid). Ecotoxicological risk assessment, of sludge application onto soils, has also been evaluated. Risk quotients, expressed as the ratio between the predicted environmental concentration and the predicted non-effect concentration, were lower than 1 for all the pharmaceutically active compounds so no significant risks are expected to occur due to the application of sewage sludge onto soils, except for 17?-ethinylestradiol when chronic toxicity was considered. PMID:24909712

  2. 78 FR 11119 - Air Quality: Revision to Definition of Volatile Organic Compounds-Exclusion of trans

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-02-15

    ...of volatile organic compounds (VOCs) for purposes...E)) to the list of compounds excluded from the definition...the basis that this compound makes a negligible contribution...E)) to the list of compounds excluded from the definition...the basis that this compound makes a...

  3. Spatial Arrangment of Organic Compounds on a Model Mineral Surface: Implications for Soil Organic Matter Stabilization

    SciTech Connect

    Petridis, Loukas; Ambaye, Haile Arena; Jagadamma, Sindhu; Kilbey, S. Michael; Lokitz, Bradley S; Lauter, Valeria; Mayes, Melanie

    2014-01-01

    The complexity of the mineral organic carbon interface may influence the extent of stabilization of organic carbon compounds in soils, which is important for global climate futures. The nanoscale structure of a model interface was examined here by depositing films of organic carbon compounds of contrasting chemical character, hydrophilic glucose and amphiphilic stearic acid, onto a soil mineral analogue (Al2O3). Neutron reflectometry, a technique which provides depth-sensitive insight into the organization of the thin films, indicates that glucose molecules reside in a layer between Al2O3 and stearic acid, a result that was verified by water contact angle measurements. Molecular dynamics simulations reveal the thermodynamic driving force behind glucose partitioning on the mineral interface: The entropic penalty of confining the less mobile glucose on the mineral surface is lower than for stearic acid. The fundamental information obtained here helps rationalize how complex arrangements of organic carbon on soil mineral surfaces may arise

  4. Comparison of organic peracids in wastewater treatment: Disinfection, oxidation and corrosion.

    PubMed

    Luukkonen, Tero; Heyninck, Tom; Rämö, Jaakko; Lassi, Ulla

    2015-11-15

    The use of organic peracids in wastewater treatment is attracting increasing interest. The common beneficial features of peracids are effective anti-microbial properties, lack of harmful disinfection by-products and high oxidation power. In this study performic (PFA), peracetic (PAA) and perpropionic acids (PPA) were synthesized and compared in laboratory batch experiments for the inactivation of Escherichia coli and enterococci in tertiary wastewater, oxidation of bisphenol-A and for corrosive properties. Disinfection tests revealed PFA to be a more potent disinfectant than PAA or PPA. 1.5 mg L(-1) dose and 2 min of contact time already resulted in 3.0 log E. coli and 1.2 log enterococci reduction. Operational costs of disinfection were estimated to be 0.0114, 0.0261 and 0.0207 €/m(3) for PFA, PAA and PPA, respectively. Disinfection followed the first order kinetics (Hom model or S-model) with all studied peracids. However, in the bisphenol-A oxidation experiments involving Fenton-like conditions (pH = 3.5, Fe(2+) or Cu(2+) = 0.4 mM) peracids brought no additional improvement to traditionally used and lower cost hydrogen peroxide. Corrosion measurements showed peracids to cause only a negligible corrosion rate (<6 ?m year(-1)) on stainless steel 316L while corrosion rates on the carbon steel sample were significantly higher (<500 ?m year(-1)). PMID:26342181

  5. LEVELS OF SYNTHETIC MUSKS COMPOUNDS IN MUNICIPAL WASTEWATER FOR ESTIMATING BIOTA EXPOSURE IN RECEIVING WATERS

    EPA Science Inventory

    Synthetic musk compounds are consumer chemicals manufactured as fragrance materials and consumed in very large quantities worldwide. Due to their high use and release, they have become ubiquitous in the environment. We analyzed water samples from the confluence of three municipal...

  6. LEVELS OF SYNTHETIC MUSK COMPOUNDS IN MUNICIPAL WASTEWATER FOR ESTIMATION OF BIOTA EXPOSURE IN RECEIVING WATERS

    EPA Science Inventory

    To be presented is an overview of the chemistry, the monitoring methodology, and the statistical evaluation of concentrations obtained from the analysis of a suite of compounds (e.g., Galaxolide®, musk xylene, and amino musk xylene) in an aquatic ecological site.

  7. DETERMINATION OF SYNTHETIC MUSK COMPOUNDS IN MUNICIPAL WASTEWATER AND ESTIMATING BIOTA EXPOSURE IN THE RECEIVING WATERS

    EPA Science Inventory

    Synthetic musk compounds are consumer chemicals manufactured as fragrance materials and consumed in very large quantities worldwide. Due to their high usage and release, they have become ubiquitous in the environment. The U.S. EPA (Las Vegas) developed surface water monitoring me...

  8. The Differentiation of Biodegradable and Non-Biodegradable Dissolved Organic Matter in Wastewaters Using Fluorescence and Raman Scattering Data}

    NASA Astrophysics Data System (ADS)

    Reynolds, D. M.

    2006-12-01

    The chemical and biochemical oxygen demand values of a number of synthetic and wastewater samples were determined using fluorescence spectroscopy. Treated and untreated wastewater samples were obtained from a local sewage treatment works while synthetic samples were treated via a rotating biodisc contactor. Fluorescence intensities were normalised using the water Raman signal as an internal standard and corrections applied to take into account the attenuation effects caused by the sample matrix. The fluorescence properties (? exc = 280nm) of synthetic and wastewater samples exhibited major similarities regarding their fluorescence response. Two main fluorescence bands centred around 350 nm and 440 nm were observed in all samples. Normalised fluorescence data, centred at 350 nm, correlate well with corresponding BOD, COD and TOC values (R2 values ranging between 0.93 and 0.98). Using BOD, COD and TOC data the fluorescence at 350nm and 440 nm can be apportioned to biodegradable and non-biodegradable dissolved organic matter respectively. The findings of this research show that fluorescence and Raman scattering data can be used to quantify chemical and biochemical oxygen demand values of wastewater. Furthermore the spectral data can be apportioned to biodegradable (BOD) and non-biodegradable (COD-BOD) dissolved organic matter. The potential of using fluorescence spectroscopy as a possible tool for real-time monitoring of sewage wastes is discussed. Key words - fluorescence, biodegradable, non-biodegradable, synthetic sewage, wastewater, monitoring

  9. Identification of characteristic organic contaminants in wastewaters from modern paper production sites and subsequent tracing in a river.

    PubMed

    Dsikowitzky, Larissa; Botalova, Oxana; Illgut, Sarah; Bosowski, Sylwana; Schwarzbauer, Jan

    2015-12-30

    The paper industry is one of the most significant industrial branches that contributes to water pollution. Recent studies regarding the chemical composition of wastewaters from modern paper production sites are sparse, and organic contaminants originating from this source may remain undetected and uncontrolled. Therefore, for this study, non-target screening analyses of wastewaters from five different paper production sites were performed, including an extended analysis of one facility, for the identification of volatile non-polar to semi-polar organic contaminants. The identified contaminants were also traced in the adjacent river. Several specific agents related to paper production, including photoinitiators, ink and thermal paper constituents, were present in most wastewaters and were therefore considered to be characteristic paper industry contaminants. A couple of contaminants identified in this study are being reported for the first time and might be toxic, but have been neglected in previous studies. Bisphenol A and 2,4,7,9-tetramethyl-5-decyne-4,7-diol were found in untreated wastewaters, treated wastewater and in river water. Bisphenol A was present in river water downstream from where the paper industry discharges at a concentration that was reported to affect the reproduction of gastropods. Thus, our findings imply that paper industry discharges pose a risk to the populations of sensitive macroinvertebrates. PMID:26188868

  10. Racemization and the origin of optically active organic compounds in living organisms

    NASA Technical Reports Server (NTRS)

    Bada, J. L.; Miller, S. L.

    1987-01-01

    The organic compounds synthesized in prebiotic experiments are racemic mixtures. A number of proposals have been offered to explain how asymmetric organic compounds formed on the Earth before life arose, with the influence of chiral weak nuclear interactions being the most frequent proposal. This and other proposed asymmetric syntheses give only sight enantiomeric excess and any slight excess will be degraded by racemization. This applies particularly to amino acids where half-lives of 10(5)-10(6) years are to be expected at temperatures characteristic of the Earth's surface. Since the generation of chiral molecules could not have been a significant process under geological conditions, the origins of this asymmetry must have occurred at the time of the origin of life or shortly thereafter. It is possible that the compounds in the first living organisms were prochiral rather than chiral; this is unlikely for amino acids, but it is possible for the monomers of RNA-like molecules.

  11. THE OXIDATION OF ORGANIC COMPOUNDS IN THE TROPOSPHERE AND THEIR GLOBAL WARMING POTENTIALS

    E-print Network

    Stevenson, David

    pulses of 10 organic compounds were followed in a global 3-D Lagrangian chemistry-transport modelTHE OXIDATION OF ORGANIC COMPOUNDS IN THE TROPOSPHERE AND THEIR GLOBAL WARMING POTENTIALS W. J by hydroxyl radicals is the main removal process for organic compounds in the troposphere. This oxidation acts

  12. 78 FR 11101 - Air Quality: Revision to Definition of Volatile Organic Compounds-Exclusion of trans

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-02-15

    ... Volatile Organic Compounds in Ozone State Implementation Plans'' (Interim Guidance) (70 FR 54046, September... volatile organic compounds in ozone state implementation plans. 70 FR 54046-54051, September 15, 2005. U.S... definition was first set forth in the ``Recommended Policy on Control of Volatile Organic Compounds'' (42...

  13. Dehalogenation of chlorinated organic compounds by strong alkalis

    SciTech Connect

    Gu, B.; Siegrist, R.L.

    1997-10-01

    Chlorinated organic compounds such as trichloroethylene (TCE) are the most prevalent contaminants found in soil and ground water, and pose serious health risks even at trace concentrations. This research reports a new chemical treatment technique for rapid degradation of TCE in strong alkaline solutions. Batch kinetic reactions between TCE and NaOH indicate that TCE can be rapidly and completely dechlorinated in NaOH at elevated temperatures. The reaction can be described by a pseudo-first-order rate kinetics with an estimated activation energy of {approximately}85 kJ/mol. The half-lives for TCE degradation in 2M NaOH at 40, 60, 80, and 100 C were approximately 347, 48.8, 4.0, and 2.4 min, respectively. The reaction end-products are primarily Cl{sup {minus}} anions and Na-glycollate, both of which are nonhazardous. This treatment technique is applicable for degrading other halogenated organic compounds wherein a nucleophilic substitution or elimination is the major reaction mechanism or pathway. Potential applications of this technology include the removal and destruction of vapor-phase chlorinated volatile organic compounds (VOCs) in off-gases when soil vapor extraction or air-stripping techniques are used for remediating VOC-contaminated soils and ground water. A bench-scale alkaline destruction module was tested, and results indicated that {approximately}90% of TCE was destroyed when TCE vapor (10 mg/L) was passed through a destruction column with a retention time of {approximately}1 min at 95 C.

  14. The synthesis of organic and inorganic compounds in evolved stars.

    PubMed

    Kwok, Sun

    2004-08-26

    Recent isotopic analysis of meteorites and interplanetary dust has identified solid-state materials of pre-solar origin. We can now trace the origin of these inorganic grains to the circumstellar envelopes of evolved stars. Moreover, organic (aromatic and aliphatic) compounds have been detected in proto-planetary nebulae and planetary nebulae, which are the descendants of carbon stars. This implies that molecular synthesis is actively happening in the circumstellar environment on timescales as short as several hundred years. The detection of stellar grains in the Solar System suggests that they can survive their journey through the interstellar medium and that they are a major contributor of interstellar grains. PMID:15329712

  15. Semivolatile organic compounds in the atmosphere: a review

    SciTech Connect

    Harkov, R.

    1986-01-01

    Semivolatile organic pollutants (SVOP) have been linked to lung cancer mortality incidence in both the workplace and ambient environment. However, as a result of the complex nature of SVOP it has been very difficult to link specific classes of compounds with health effects in defined human populations. The present report outlines health effects, collection and analysis information pertaining to SVOP and is an attempt to highlight where improvements in the state-of-knowledge on these materials is clearly needed. A case study approach is utilized to characterize methodological approaches to the study of SVOP in ambient and source samples. 157 references.

  16. Volatile organic compounds in storm water from a parking lot

    USGS Publications Warehouse

    Lopes, T.J.; Fallon, J.D.; Rutherford, D.W.; Hiatt, M.H.

    2000-01-01

    A mass balance approach was used to determine the most important nonpoint source of volatile organic compounds (VOCs) in storm water from an asphalt parking lot without obvious point sources (e.g., gasoline stations). The parking lot surface and atmosphere are important nonpoint sources of VOCs, with each being important for different VOCs. The atmosphere is an important source of soluble, oxygenated VOCs (e.g., acetone), and the parking lot surface is an important source for the more hydrophobic VOCs (e.g., benzene). VOCs on the parking lot surface appear to be concentrated in oil and grease and organic material in urban particles (e.g., vehicle soot). Except in the case of spills, asphalt does not appear to be an important source of VOCs. The uptake isotherm of gaseous methyl tert-butyl ether on urban particles indicates a mechanism for dry deposition of VOCs from the atmosphere. This study demonstrated that a mass balance approach is a useful means of understanding non-point-source pollution, even for compounds such as VOCs, which are difficult to sample.A mass balance approach was used to determine the most important nonpoint source of volatile organic compounds (VOCs) in storm water from an asphalt parking lot without obvious point sources (e.g., gasoline stations). The parking lot surface and atmosphere are important nonpoint sources of VOCs, with each being important for different VOCs. The atmosphere is an important source of soluble, oxygenated VOCs (e.g., acetone), and the parking lot surface is an important source for the more hydrophobic VOCs (e.g., benzene). VOCs on the parking lot surface appear to be concentrated in oil and grease and organic material in urban particles (e.g., vehicle soot). Except in the case of spills, asphalt does not appear to be an important source of VOCs. The uptake isotherm of gaseous methyl tert-butyl ether on urban particles indicates a mechanism for dry deposition of VOCs from the atmosphere. This study demonstrated that a mass balance approach is a useful means of understanding non-point-source pollution, even for compounds such as VOCs, which are difficult to sample.

  17. EMISSION OF METALS AND ORGANICS FROM MUNICIPAL WASTEWATER SLUDGE INCINERATORS - VOLUME VIII: GC/MS TAPES REVIEW REPORT

    EPA Science Inventory

    Emissions of metals and organics from a series of four municipal wastewater sludge incinerators were determined. hree multiple hearth units and one fluidized bed combustor were tested. missions were controlled with a combination of venturi and/or tray impingement scrubbers. ne si...

  18. Demonstrating sucralose as a monitor of full-scale UV/AOP treatment of trace organic compounds.

    PubMed

    Lester, Yaal; Ferrer, Imma; Thurman, E Michael; Linden, Karl G

    2014-09-15

    Due to the large number of trace organic compounds (TOrCs) in water and wastewater, their degradation during UV-based advanced oxidation (UV/AOP) is best monitored using a conservative indicator compound. The present study demonstrates the in situ use of sucralose, a widely consumed artificial sweetener, as a conservative probe for UV/AOP degradation of TOrCs. The main qualities of sucralose in this regard are its high concentration in wastewater effluent and surface water (enabling its direct detection), its resistance to direct UV photolysis, and its relatively slow reaction with hydroxyl radical. Degradation of sucralose was compared to the degradation of commonly detected TOrCs, across two AOPs (i.e. UV/H2O2 and UV/NO3), in both lab-scale and pilot-scale systems. In all cases, UV/AOP degradation of sucralose was slower than the degradation of the examined TOrCs, and is expected to be slower than the degradation of the majority of other environmentally relevant TOrCs. These results demonstrate the potential of sucralose as a conservative probe, to monitor the transformation of TOrCs during UV/AOP treatment. Furthermore, degradation of sucralose was slower than the degradation of many transformation products (generated during oxidation of TOrCs), implying that sucralose is also a valuable indicator for the decay of primary transformation products. PMID:25146095

  19. ORGANIC CATION EFFECTS ON THE SORPTION OF METALS AND NEUTRAL ORGANIC COMPOUNDS ON AQUIFER MATERIAL (JOURNAL VERSION)

    EPA Science Inventory

    Sorption of ethylhexadecyldimethylammonium (EHDDMA+), a large organic cation, and three neutral organic compounds (NOC's) on two low organic carbon aquifer materials was studied using a soil batch equilibration technique. EHDDMA+ competed effectively with metals for exchange site...

  20. Volatilization modeling of semivolatile organic compounds during solidification processes

    SciTech Connect

    Sass, B.M.; Smith, L.A. Huang, W.M.C.; Rosansky, S.H.; Drescher, E.

    1996-12-31

    Technical information is provided on the effects of temperature elevation on increasing the volatility of semivolatile organic compounds (SVOCs) in stabilization media. A chemical diffusion model was developed (1) to establish a technical basis for determining maximum treatment temperatures above which SVOCs should not be exposed during solidification processes to reduce the potential for unacceptable releases; and (2) to prescribe types of binders with sufficiently low heat output to stabilize organics that have potential for volatilizing with moderate heating, and to recommend against use of others that may not maintain the mixture at sufficiently low temperatures. A non-steady-state model for linear diffusion in the aqueous and vapor phase was used because the SVOC dynamics of diffusion are controlled by resistances in both pore water and air. The results of volatilization calculations performed are presented.

  1. Marine Vibrio Species Produce the Volatile Organic Compound Acetone

    PubMed Central

    Nemecek-Marshall, M.; Wojciechowski, C.; Kuzma, J.; Silver, G. M.; Fall, R.

    1995-01-01

    While screening aerobic, heterotrophic marine bacteria for production of volatile organic compounds, we found that a group of isolates produced substantial amounts of acetone. Acetone production was confirmed by gas chromatography, gas chromatography-mass spectrometry, and high-performance liquid chromatography. The major acetone producers were identified as nonclinical Vibrio species. Acetone production was maximal in the stationary phase of growth and was stimulated by addition of l-leucine but not the other common amino acids, suggesting that leucine degradation leads to acetone formation. Acetone production by marine vibrios may contribute to the dissolved organic carbon associated with phytoplankton, and some of the acetone produced may be volatilized to the atmosphere. PMID:16534920

  2. Thermodynamics of Aqueous Organic Sulfur Compounds: A Key to the Organic Geochemistry of Hydrothermal Systems?

    NASA Technical Reports Server (NTRS)

    Schulte, Mitchell; Rogers, Karyn L.; DeVincenzi, Donald L. (Technical Monitor)

    2000-01-01

    Hydrothermal environments are locations of varied geochemistry due to the disequilibrium between vent fluids and seawater. The disequilibrium geochemistry has been hypothesized to include reactions to synthesize organic compounds. Observations of the organic geochemistry of hydrothermal vent sites has received little attention. Experimental simulations of these environments, however, indicate that organic compounds may have difficulty forming in a purely aqueous environment. On the other hand, thiols. thioesters and disulfides have been implicated as reaction intermediates between CO or CO2 in experiments of carbon reduction in hydrothermal environments as well as in a variety of biological processes and other abiotic reactions (Wachtershauser, 1990, OLEB 20, 173; Heinen and Lauwers, 1996, OLEB 26, 13 1, Huber and Wachtershauser, 1997, Science 276, 245; Russell et al., 1998, in Thermophiles: The keys to molecular evolution and the origin of life?). The reduction of CO2 to thiols, for example, is observed using the FeS-H2S/FeS2 couple to provide the reducing power (see Schoonen et al., 1999, OLEB 29, 5). In addition, the enzyme involved in final stage of methanogenesis, coenzyme-M, is itself a thiol. Thus, organic sulfur compounds may hold the key to the organic chemistry leading to the origin of life at high temperatures. Understanding the biochemical processes of microorganisms that can live to temperatures at least as high as 113 C (Blochl et al., 1996, Extremophiles 1, 14) requires knowledge of the properties of the chemical reactions involved. In order to assess the role of aqueous organic sulfur compounds in hydrothermal organic geochemistry, we have been attempting to determine their thermodynamic properties. We have culled the literature to obtain the properties of organic sulfur compounds. We are able to calculate a number of essential properties, such as free energies of formation, from solubility data available in the literature together with standard properties of organic sulfur gases. However, a number of the properties for aqueous organic sulfur compounds have not been experimentally determined. Furthermore, most of thermodynamic data that are available are for 25 C and 1 bar. In order to determine reaction properties to temperatures and pressures appropriate to the hydrothermal conditions in which thermophilic organisms actually live, we use equations of state developed by Helgeson and co-workers (Helgeson et al., 1981, AJS 281, 1249). A key piece of information needed to go up in temperature is the partial molal heat capacity, which is one of the properties for which experimental data are unavailable for nearly all organic sulfur compounds. We have used correlation methods to determine the partial molal heat capacities and volumes of many organic solutes. These estimates allow us to asses the role of organic sulfur compounds during the reduction of carbon in hydrothermal settings. We will present these data, along with examples of the thermodynamic properties of reactions involving aqueous organic sulfur compounds.

  3. [Simultaneous removal of carbon and nitrogen from organic-rich wastewater with Anammox].

    PubMed

    Chen, Chongjun; Zhu, Weijing; Huang, Xiaoxiao; Wu, Weixiang

    2014-12-01

    In order to simultaneously remove carbon and nitrogen from organic-rich wastewater, we used an up-flow anaerobic sludge bed/blanket (UASB) reactor that was started up with anammox with high concentration of carbon and nitrogen by gradually raising the organic loading of influent. We optimized the removal of nitrogen and carbon when the chemical oxygen demand (COD) concentration varied from 172 to 620 mg/L. During the entire experiment, the ammonium and total nitrogen removal efficiency was higher than 85%, while the average COD removal efficiency was 56.6%. The high concentration of organic matter did not restrain the activity of anammox bacteria. Based on polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) and tapping sequencing analyses, the Planctomycete, Proteobacteria, Chloroflexi, Chlorobi bacteria are detected in the UASB reactor, which indicated complex removal pathway of carbon and nitrogen coexisted in the reactor. However, a part of Planctomycete which referred to anammox bacteria could tolerate a high content of organic carbon, and it provided help for high performance of nitrogen removal in UASB reactor. PMID:26016373

  4. Organics removal of combined wastewater through shallow soil infiltration treatment: a field and laboratory study.

    PubMed

    Zhang, Zhiyin; Lei, Zhongfang; Zhang, Zhenya; Sugiura, Norio; Xu, Xiaotian; Yin, Didi

    2007-11-19

    Soil infiltration treatment (SIT) was proved to be an effective and low-cost treatment technique for decentralized effluents in the areas without perfect sewage systems. Field-scale experiments were conducted under several conditions to assess organics removals through a shallow soil infiltration treatment (SSIT, with effective depth 0.3m) of combined wastewater (discharge from toilets, restaurants and a gas station), while bench-scale soil column experiments were performed in laboratory in parallel to investigate biological and abiological effects of this kind of system. From the start-up to the 10th month, the field SSIT trenches experienced the lowest and highest temperatures of the operation period in Shanghai and exhibited effective organics removals after maturation, with the highest removal rate 75.8% of chemical oxygen demand (COD), highest ultraviolet absorption at 254 nm (UV(254)) decrease by 67.2% and 35.2-100% removals of phenolic and phthalate pollutants. The laboratory results indicated that more organics could be removed in room-temperatured (25+/-2 degrees C) SSIT systems under different influent COD concentrations from 45 mg/l to 406 mg/l, and the highest total COD removal rate could reach 94.0%, in which biological effect accounted for 57.7-71.9%. The results showed that temperature and hydraulic loading rate were the most important factors influencing the removals of COD and organic pollutants in SSIT. PMID:17512114

  5. Are Some Fungal Volatile Organic Compounds (VOCs) Mycotoxins?

    PubMed Central

    Bennett, Joan W.; Inamdar, Arati A.

    2015-01-01

    Volatile organic compounds (VOCs) are carbon-compounds that easily evaporate at room temperature. Toxins are biologically produced poisons; mycotoxins are those toxins produced by microscopic fungi. All fungi emit blends of VOCs; the qualitative and quantitative composition of these volatile blends varies with the species of fungus and the environmental situation in which the fungus is grown. These fungal VOCs, produced as mixtures of alcohols, aldehydes, acids, ethers, esters, ketones, terpenes, thiols and their derivatives, are responsible for the characteristic moldy odors associated with damp indoor spaces. There is increasing experimental evidence that some of these VOCs have toxic properties. Laboratory tests in mammalian tissue culture and Drosophila melanogaster have shown that many single VOCs, as well as mixtures of VOCs emitted by growing fungi, have toxic effects. This paper describes the pros and cons of categorizing toxigenic fungal VOCs as mycotoxins, uses genomic data to expand on the definition of mycotoxin, and summarizes some of the linguistic and other conventions that can create barriers to communication between the scientists who study VOCs and those who study toxins. We propose that “volatoxin” might be a useful term to describe biogenic volatile compounds with toxigenic properties. PMID:26402705

  6. Volatile organic compounds adsorption onto neat and hybrid bacterial cellulose

    NASA Astrophysics Data System (ADS)

    Ion, Violeta Alexandra; Pârvulescu, Oana Cristina; Dobre, T?nase

    2015-04-01

    Adsorption dynamics of VOCs (volatile organic compounds) vapour from air streams onto fixed bed adsorbent were measured and simulated under various operation conditions. Isopropanol (IPA) and n-hexane (HEX) were selected as representatives of polar and nonpolar VOCs, whereas bacterial cellulose (BC) and BC incorporated with magnetite nanoparticles (M/BC), were tested as adsorbents. An experimental study emphasizing the influence of air superficial velocity (0.7 cm/s and 1.7 cm/s), operation temperature (30 °C and 40 °C), adsorbate and adsorbent type, on fixed bed saturation curves was conducted. Optimal adsorption performances evaluated in terms of saturation adsorption capacity were obtained for the adsorption of polar compound (IPA) onto M/BC composite (0.805 g/g) and of nonpolar compound (HEX) onto neat BC (0.795 g/g), respectively, at high values of air velocity and operation temperature. A mathematical model including mass balance of VOC species, whose parameters were fitted based on experimental data, was developed in order to predict the fixed bed saturation curves. A 23 statistical model indicating a significant increase in adsorption performances with process temperature was validated under the experimental conditions.

  7. Methods in plant foliar volatile organic compounds research1

    PubMed Central

    Materi?, Dušan; Bruhn, Dan; Turner, Claire; Morgan, Geraint; Mason, Nigel; Gauci, Vincent

    2015-01-01

    Plants are a major atmospheric source of volatile organic compounds (VOCs). These secondary metabolic products protect plants from high-temperature stress, mediate in plant–plant and plant–insect communication, and affect our climate globally. The main challenges in plant foliar VOC research are accurate sampling, the inherent reactivity of some VOC compounds that makes them hard to detect directly, and their low concentrations. Plant VOC research relies on analytical techniques for trace gas analysis, usually based on gas chromatography and soft chemical ionization mass spectrometry. Until now, these techniques (especially the latter one) have been developed and used primarily by physicists and analytical scientists, who have used them in a wide range of scientific research areas (e.g., aroma, disease biomarkers, hazardous compound detection, atmospheric chemistry). The interdisciplinary nature of plant foliar VOC research has recently attracted the attention of biologists, bringing them into the field of applied environmental analytical sciences. In this paper, we review the sampling methods and available analytical techniques used in plant foliar VOC research to provide a comprehensive resource that will allow biologists moving into the field to choose the most appropriate approach for their studies. PMID:26697273

  8. Are Some Fungal Volatile Organic Compounds (VOCs) Mycotoxins?

    PubMed

    Bennett, Joan W; Inamdar, Arati A

    2015-09-01

    Volatile organic compounds (VOCs) are carbon-compounds that easily evaporate at room temperature. Toxins are biologically produced poisons; mycotoxins are those toxins produced by microscopic fungi. All fungi emit blends of VOCs; the qualitative and quantitative composition of these volatile blends varies with the species of fungus and the environmental situation in which the fungus is grown. These fungal VOCs, produced as mixtures of alcohols, aldehydes, acids, ethers, esters, ketones, terpenes, thiols and their derivatives, are responsible for the characteristic moldy odors associated with damp indoor spaces. There is increasing experimental evidence that some of these VOCs have toxic properties. Laboratory tests in mammalian tissue culture and Drosophila melanogaster have shown that many single VOCs, as well as mixtures of VOCs emitted by growing fungi, have toxic effects. This paper describes the pros and cons of categorizing toxigenic fungal VOCs as mycotoxins, uses genomic data to expand on the definition of mycotoxin, and summarizes some of the linguistic and other conventions that can create barriers to communication between the scientists who study VOCs and those who study toxins. We propose that "volatoxin" might be a useful term to describe biogenic volatile compounds with toxigenic properties. PMID:26402705

  9. Methods in plant foliar volatile organic compounds research.

    PubMed

    Materi?, Dušan; Bruhn, Dan; Turner, Claire; Morgan, Geraint; Mason, Nigel; Gauci, Vincent

    2015-12-01

    Plants are a major atmospheric source of volatile organic compounds (VOCs). These secondary metabolic products protect plants from high-temperature stress, mediate in plant-plant and plant-insect communication, and affect our climate globally. The main challenges in plant foliar VOC research are accurate sampling, the inherent reactivity of some VOC compounds that makes them hard to detect directly, and their low concentrations. Plant VOC research relies on analytical techniques for trace gas analysis, usually based on gas chromatography and soft chemical ionization mass spectrometry. Until now, these techniques (especially the latter one) have been developed and used primarily by physicists and analytical scientists, who have used them in a wide range of scientific research areas (e.g., aroma, disease biomarkers, hazardous compound detection, atmospheric chemistry). The interdisciplinary nature of plant foliar VOC research has recently attracted the attention of biologists, bringing them into the field of applied environmental analytical sciences. In this paper, we review the sampling methods and available analytical techniques used in plant foliar VOC research to provide a comprehensive resource that will allow biologists moving into the field to choose the most appropriate approach for their studies. PMID:26697273

  10. 40 CFR Table 1 to Subpart B of... - Volatile Organic Compound (VOC) Content Limits for Automobile Refinish Coatings

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...2013-07-01 2013-07-01 false Volatile Organic Compound (VOC) Content Limits for Automobile...PROGRAMS (CONTINUED) NATIONAL VOLATILE ORGANIC COMPOUND EMISSION STANDARDS FOR CONSUMER AND COMMERCIAL PRODUCTS National Volatile Organic Compound Emission Standards for...

  11. 40 CFR Table 1 to Subpart B of... - Volatile Organic Compound (VOC) Content Limits for Automobile Refinish Coatings

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...2014-07-01 2014-07-01 false Volatile Organic Compound (VOC) Content Limits for Automobile...PROGRAMS (CONTINUED) NATIONAL VOLATILE ORGANIC COMPOUND EMISSION STANDARDS FOR CONSUMER AND COMMERCIAL PRODUCTS National Volatile Organic Compound Emission Standards for...

  12. 40 CFR Table 1 to Subpart B of... - Volatile Organic Compound (VOC) Content Limits for Automobile Refinish Coatings

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...2012-07-01 2012-07-01 false Volatile Organic Compound (VOC) Content Limits for Automobile...PROGRAMS (CONTINUED) NATIONAL VOLATILE ORGANIC COMPOUND EMISSION STANDARDS FOR CONSUMER AND COMMERCIAL PRODUCTS National Volatile Organic Compound Emission Standards for...

  13. 40 CFR Table 1 to Subpart B of... - Volatile Organic Compound (VOC) Content Limits for Automobile Refinish Coatings

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 2011-07-01 false Volatile Organic Compound (VOC) Content Limits for Automobile...PROGRAMS (CONTINUED) NATIONAL VOLATILE ORGANIC COMPOUND EMISSION STANDARDS FOR CONSUMER AND COMMERCIAL PRODUCTS National Volatile Organic Compound Emission Standards for...

  14. 40 CFR Table 1 to Subpart B of... - Volatile Organic Compound (VOC) Content Limits for Automobile Refinish Coatings

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...2010-07-01 false Volatile Organic Compound (VOC) Content Limits for Automobile...CONTINUED) NATIONAL VOLATILE ORGANIC COMPOUND EMISSION STANDARDS FOR CONSUMER AND COMMERCIAL PRODUCTS National Volatile Organic Compound Emission Standards for Automobile...

  15. Anti-photoaging and Photoprotective Compounds Derived from Marine Organisms

    PubMed Central

    Pallela, Ramjee; Na-Young, Yoon; Kim, Se-Kwon

    2010-01-01

    Marine organisms form a prominent component of the oceanic population, which significantly contribute in the production of cosmeceutical and pharmaceutical molecules with biologically efficient moieties. In addition to the molecules of various biological activities like anti-bacterial, anti-cancerous, anti-inflammatory and anti-oxidative etc., these organisms also produce potential photoprotective or anti-photoaging agents, which are attracting present day researchers. Continuous exposure to UV irradiation (both UV-A and UV-B) leads to the skin cancer and other photoaging complications, which are typically mediated by the reactive oxygen species (ROS), generated in the oxidative pathways. Many of the anti-oxidative and anti-photoaging compounds have been identified previously, which work efficiently against photodamage of the skin. Recently, marine originated photoprotective or anti-photoaging behavior was observed in the methanol extracts of Corallina pilulifera (CPM). These extracts were found to exert potent antioxidant activity and protective effect on UV-A-induced oxidative stress in human dermal fibroblast (HDF) cells by protecting DNA and also by inhibiting matrix metalloproteinases (MMPs), a key component in photoaging of the skin due to exposure to UV-A. The present review depicts various other photoprotective compounds from algae and other marine sources for further elaborative research and their probable use in cosmeceutical and pharmaceutical industries. PMID:20479974

  16. Biogenic volatile organic compound emissions from vegetation fires

    PubMed Central

    CICCIOLI, PAOLO; CENTRITTO, MAURO; LORETO, FRANCESCO

    2014-01-01

    The aim of this paper was to provide an overview of the current state of the art on research into the emission of biogenic volatile organic compounds (BVOCs) from vegetation fires. Significant amounts of VOCs are emitted from vegetation fires, including several reactive compounds, the majority belonging to the isoprenoid family, which rapidly disappear in the plume to yield pollutants such as secondary organic aerosol and ozone. This makes determination of fire-induced BVOC emission difficult, particularly in areas where the ratio between VOCs and anthropogenic NOx is favourable to the production of ozone, such as Mediterranean areas and highly anthropic temperate (and fire-prone) regions of the Earth. Fire emissions affecting relatively pristine areas, such as the Amazon and the African savannah, are representative of emissions of undisturbed plant communities. We also examined expected BVOC emissions at different stages of fire development and combustion, from drying to flaming, and from heatwaves coming into contact with unburned vegetation at the edge of fires. We conclude that forest fires may dramatically change emission factors and the profile of emitted BVOCs, thereby influencing the chemistry and physics of the atmosphere, the physiology of plants and the evolution of plant communities within the ecosystem. PMID:24689733

  17. Treatment and reuse of coal conversion wastewaters

    SciTech Connect

    Luthy, R.G.

    1980-01-01

    This paper presents a synopsis of recent experimental activities to evaluate processing characteristics of coal conversion wastewaters. Treatment studies have been performed with high-BTU coal gasification process quench waters to assess enhanced removal of organic compounds via powdered activated carbon-activated sludge treatment, and to evaluate a coal gasification wastewater treatment train comprised of sequential processing by ammonia removal, biological oxidation, lime-soda softening, granular activated carbon adsorption, and reverse osmosis. In addition, treatment studies are in progress to evaluate solvent extraction of gasification process wastewater to recover phenolics and to reduce wastewater loading of priority organic pollutants. Biological oxidation of coal gasification wastewater has shown excellent removal efficiencies of major and trace organic contaminants at moderate loadings, addition of powdered activated carbon provides lower effluent COD and color. Gasification process wastewater treated through biological oxidation, lime-soda softening and activated carbon adsorption appears suitable for reuse as cooling tower make-up water. Solvent extraction is an effective means to reduce organic loadings to downstream processing units. In addition, preliminary results have shown that solvent extraction removes chromatographable organic contaminants to low levels.

  18. Determination of selenium and its compounds in marine organisms.

    PubMed

    Bryszewska, Ma?gorzata Anita; Mĺge, Amund

    2015-01-01

    In this study, we investigate the type and quantity of selenium compounds in fish and marine organisms, using ion-pair reversed phase LC–ICP-MS, developed and applied for the analysis of Atlantic cod, Atlantic salmon, Greenland halibut, Atlantic herring, blue mussel, common crab, scallop, calanus, and Euphasia super. Of the samples examined, the lowest level of selenium was found in farmed Atlantic salmon (0.17 mg Se kg(?1) dm). The total selenium extraction efficiency by phosphate buffer was 2.5 times higher in sea plankton and shellfish samples than in fish samples. Analysis of Se species in each hydrolysate obtained by proteolysis showed the presence of selenomethionine, which constituted 41.5% of the selenium compounds detected in hydrolysates of Atlantic herring and 98.4% of those in extracts of Atlantic salmon. Inorganic compounds, such as selenates and selenites, were detected mainly in sea plankton and shellfish samples (<0.13 mg Se kg(?1) wm), although no correlation was found between the presence of inorganic compounds and total selenium concentration. The accuracy of the total selenium determination was validated using a certified reference material (oyster tissue (NIST 1566b)). A lyophilised powder of cod (Gadus morhua) was used to validate speciation analysis, enzymatic hydrolysis of lyophilised powder of cod recovered 54 ± 6% of total selenium, and SeMet constituted 83.5 ± 5.28% of selenium detected in hydrolysates. The chromatographic detection limits were, respectively, 0.30 ng mL(?1), 0.43 ng mL(?1), 0.54 ng mL(?1), 0.55 ng mL(?1), 0.57 ng mL(?1) and 0.72 ng mL(?1) for selenate, selenomethionine, selenite, Se-methyl-selenocysteine, selenocystine and selenomethionine selenoxide.The data on selenium concentrations and speciation presented here could be useful in estimating levels of selenium intake by seafood consumption. PMID:25468190

  19. Chiral Analyses of Organic Compounds in Carbonaceous Meteorites

    NASA Technical Reports Server (NTRS)

    Pizzarello, Sandra

    2004-01-01

    Contents include the following: 1. Characterization of Tagish Lake organic content. The first two grant years were largely devoted to the molecular and isotopic analyses of Tagish Lake organic composition. This carbonaceous meteorite fell in Canada in the winter of the year 2000, and its exceptional atmospheric entry and subsequent recovery (e. g., the sample was recovered and stored by avoiding hand contact and above freezing temperatures) contributed in providing a rare and pristine extraterrestrial material. 2. Chiral analyses of Murchison and Murray soluble organics. One of the most intriguing finding in regard to soluble meteorite organics is the presence within the amino acid suite of some compounds displaying L-enantiomeric excesses. This configuration is exclusive in the amino acids of terrestrial proteins and the finding has raised speculations of a possible role of amino acids from meteorites in the origin of homochirality on the early Earth. The main objective for this NASA funding was the characterization of enantiomeric excesses in meteorites and we have conducted several studies toward establishing their distribution and indignity.

  20. Investigation of membrane fouling in ultrafiltration using model organic compounds.

    PubMed

    Kweon, J H; Lawler, D F

    2005-01-01

    Natural organic matter (NOM) is known to be the worst foulant in the membrane processes, but the complexities of NOM make it difficult to determine its effects on membrane fouling. Therefore, simple organic compounds (surrogates for NOM) were used in this research to investigate the fouling mechanisms in ultrafiltration. Previous research on NOM components in membrane processes indicated that polysaccharides formed an important part of the fouling cake. Three polysaccharides (dextran, alginic acid, and polygalacturonic acid) and a smaller carbohydrate (tannic acid) were evaluated for their removal in softening (the treatment process in the City of Austin). Two polysaccharides (dextran and alginic acid) were selected and further investigated for their effects on membrane fouling. The two raw organic waters (4 mg/L C) showed quite different patterns of flux decline indicating different fouling mechanisms. Softening pretreatment was effective to reduce flux decline of both waters. The SEM images of the fouled membrane clearly showed the shapes of deposited foulants. The high resolution results of the XPS spectra showed substantially different spectra of carbon, C(1s), in the membrane fouled by two raw organic waters. The XPS was beneficial in determining the relative composition of each fouling material on the membrane surface. PMID:16003967